Table of Contents

 

United States

Securities and Exchange Commission

Washington, D.C. 20549

 


 

FORM 10-Q

 

 

QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended December 31, 2020September 30, 2021

or

 

 

TRANSITION REPORT PURSUANT TO SECTION 13 OR 15 (d) OF THE SECURITIES EXCHANGE ACT OF 1934

 

For the transition period from ___ to ___

 

Commission File No: 0-11740

 


 

MESA LABORATORIES, INC.

(Exact name of registrant as specified in its charter)

 

 

Colorado

 

84-0872291

 
 

(State or other jurisdiction of

 

(I.R.S. Employer

 
 

incorporation or organization)

 

Identification number)

 
     
 

12100 West Sixth Avenue

   
 

Lakewood, Colorado

 

80228

 
 

(Address of principal executive offices)

 

(Zip Code)

 

 

Registrant’s telephone number, including area code: (303) 987-8000

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each classTrading SymbolName on each exchange on which registered
Common Stock, no par valueMLABThe Nasdaq Stock Market LLC

 

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934, during the preceding 12 months (or for such shorter period that the registrant was required to file such reports) and (2) has been subject to such filing requirements for the past 90 days.

Yes ☒   No ☐

 

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (Section 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes ☒     No ☐

 

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company or an emerging growth company. See definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company” and “emerging growth company” in Rule 12b-2 of the Exchange Act.

 

Large accelerated filer ☒

Accelerated filer ☐

Non-accelerated filer ☐

Smaller reporting company ☐

Emerging growth company ☐

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act ☐

 

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act).

Yes ☐     No ☒

 

Indicate the number of shares outstanding of each of the Issuer’s classes of common stock, as of the latest practicable date:

 

There were 5,132,0035,225,232 shares of the Issuer’s common stock, no par value, outstanding as of January 28,October 29, 2021.

 



 

 

 





 

Table of Contents

 

 

 

Part I. Financial Information

1
  
 

Item 1. Financial Statements

1
 

Condensed Consolidated Balance Sheets

1
 

Condensed Consolidated Statements of OperationsIncome

2
 

Condensed Consolidated Statements of Comprehensive (Loss) Income

3
 

Condensed Consolidated Statements of Cash Flows

4
 

Condensed Consolidated Statements of Stockholders’ Equity

5
 

Notes to Condensed Consolidated Financial Statements

6
 

Item 2.  Management’s Discussion and Analysis of Financial Condition and Results of Operations

1716
 

Item 3.  Quantitative and Qualitative Disclosures about Market Risk

2523
 

Item 4.  Controls and Procedures

2623
   

Part II. Other Information

2724
  
 

Item 1.  Legal Proceedings

2724
 

Item 1A.  Risk factors

2724
 

Item 2.  Unregistered Sales of Equity Securities and Use of Proceeds

2724
 

Item 6.  Exhibits

2825
 

Signatures

2926
 

Exhibit 31.1 Certifications Pursuant to Rule 13a-14(a)

 
 

Exhibit 31.2 Certifications Pursuant to Rule 13a-14(a)

 
 

Exhibit 32.1 Certifications Pursuant to Rule 13a-14(b) and 18 U.S.C Section 1350

 
 

Exhibit 32.2 Certifications Pursuant to Rule 13a-14(b) and 18 U.S.C Section 1350

 

 

 


 

 

Part I. Financial Information

 

Item 1. Financial Statements

 

Mesa Laboratories, Inc.

Condensed Consolidated Balance Sheets

(unaudited)

(dollars in thousands, except share amounts)

 

 

December 31,

 

March 31,

  

September 30,

 

March 31,

 
 

2020

  

2020

  

2021

  

2021

 

ASSETS

            

Current assets:

          

Cash and cash equivalents

 $253,731  $81,380  $278,294  $263,865 

Accounts receivable, less allowances of $153 and $159, respectively

 20,410  21,132 

Accounts receivable, less allowances of $238 and $218, respectively

 22,636  23,787 

Inventories, net

 11,965  14,230  12,117  11,178 

Prepaid income taxes

 5,327  1,914 

Prepaid expenses and other

  3,842   4,136   6,357   4,919 

Total current assets

 295,275  122,792  319,404  303,749 

Property, plant and equipment, net of accumulated depreciation of $14,623 and $12,741, respectively

 22,295  22,066 

Property, plant and equipment, net

 22,392  21,998 

Deferred tax asset

 15,673  11,461  1,862  616 

Other assets

 1,806  2,480  1,979  2,530 

Intangibles, net

 120,803  119,871  103,488  111,741 

Goodwill

  165,784   141,536   159,977   160,841 

Total assets

 $621,636  $420,206  $609,102  $601,475 
  

LIABILITIES AND STOCKHOLDERS’ EQUITY

            

Current liabilities:

          

Accounts payable

 $3,751  $3,408  $4,463  $4,473 

Accrued payroll and benefits

 7,188  8,940  5,650  9,388 

Unearned revenues

 7,646  6,814  9,741  8,777 

Other accrued expenses

  9,165   6,846   8,836  9,945 

Total current liabilities

 27,750  26,008  28,690  32,583 

Deferred tax liability

 36,103  32,549  11,642  16,275 

Other long-term liabilities

 436  715 
Convertible senior notes, net of discounts and debt issuance costs 144,302 140,278   168,917  145,675 

Other long-term liabilities

  686   1,358 

Total liabilities

  208,841   200,193   209,685   195,248 

Stockholders’ equity:

          

Common stock, no par value; authorized 25,000,000 shares; issued and outstanding, 5,131,031 and 4,387,140 shares, respectively

 314,537  158,023 

Common stock, no par value; authorized 25,000,000 shares; issued and outstanding, 5,223,232 and 5,140,568 shares, respectively

 302,234  317,652 

Retained earnings

 69,363  72,359  82,199  72,459 

Accumulated other comprehensive income (loss)

  28,895   (10,369)

Accumulated other comprehensive income

  14,984   16,116 

Total stockholders’ equity

  412,795   220,013   399,417   406,227 

Total liabilities and stockholders’ equity

 $621,636  $420,206  $609,102  $601,475 

 

See accompanying notes to Condensed Consolidated Financial Statements.

 

Page 1


 

 

Mesa Laboratories, Inc.

Condensed Consolidated Statements of OperationsIncome

(unaudited)

(in thousands, except per share data)

 

 

Three Months Ended December 31,

  

Nine Months Ended December 31,

  

Three Months Ended September 30,

  

Six Months Ended September 30,

 
 

2020

  

2019

  

2020

  

2019

  

2021

  

2020

  

2021

  

2020

 
  

Revenues

 $34,172  $31,655  $95,973  $83,479  $35,840  $31,860  $70,760  $61,801 

Cost of revenues

  13,519   16,852   33,695   36,886   12,700   10,575   25,409   20,176 

Gross profit

 20,653  14,803  62,278  46,593  23,140  21,285  45,351  41,625 

Operating expenses:

          

Selling

 4,753  4,067  12,614  8,549  4,643  3,786  9,501  7,861 

General and administrative

 13,173  11,605  33,887  26,806  11,683  10,615  23,102  20,714 

Research and development

 2,705  2,110  7,715  4,044   2,613   2,414   5,424   5,010 
Impairment of goodwill and long-lived assets  0  276  0  298 

Total operating expenses

 20,631  18,058  54,216  39,697   18,939   16,815   38,027   33,585 

Operating income (loss)

 22  (3,255) 8,062  6,896 

Nonoperating expense:

         

Operating income

  4,201   4,470   7,324   8,040 

Nonoperating expenses:

 

Interest expense and amortization of debt discount

 1,950  1,929  5,803  3,522  815  1,934  1,629  3,853 

Other expense (income), net

  3,799   (107)  4,848   (748)
Total nonoperating expense 5,749 1,822 10,651 2,774 

(Loss) earnings before income taxes

 (5,727) (5,077) (2,589) 4,122 

Income tax (benefit) expense

  (1,185)  (573)  (1,943)  792 

Net (loss) income

 $(4,542) $(4,504) $(646) $3,330 

Other (income) expense, net

  (1,157)  152   (266)  1,049 

Total nonoperating (income) expense

  (342)  2,086   1,363   4,902 

Earnings before income taxes

 4,543  2,384  5,961  3,138 

Income tax provision (benefit)

  823   (295)  246   (758)

Net income

 $3,720  $2,679  $5,715  $3,896 
  

(Loss) earnings per share:

         

Earnings per share:

 

Basic

 $(0.89) $(1.03) $(0.13) $0.80  $0.71 $0.52 $1.10 $0.81 

Diluted

  (0.89)  (1.03)  (0.13)  0.75  $0.70 $0.51 $1.07 $0.79 
  

Weighted-average common shares outstanding:

          

Basic

 5,125  4,367  4,922  4,142  5,211  5,110  5,182  4,821 

Diluted

 5,125  4,367  4,922  4,418  5,344  5,241  5,324  4,958 

 

See accompanying notes to Condensed Consolidated Financial Statements.

 

Page 2


 

 

Mesa Laboratories, Inc.

Condensed Consolidated Statements of Comprehensive (Loss) Income

(unaudited)

(in thousands) 

 

  

Three Months Ended December 31,

  

Nine Months Ended December 31,

 
  

2020

  

2019

  

2020

  

2019

 
                 

Net (loss) income

 $(4,542) $(4,504) $(646) $3,330 

Other comprehensive income:

                

Foreign currency translation adjustments

  21,142   6,615   39,264   5,750 

Comprehensive income

 $16,600  $2,111  $38,618  $9,080 
  

Three Months Ended September 30,

  

Six Months Ended September 30,

 
  

2021

  

2020

  

2021

  

2020

 
                 

Net income

 $3,720  $2,679  $5,715  $3,896 

Other comprehensive (loss) income:

                

Foreign currency translation adjustments

  (6,503)  5,262   (1,132)  18,122 

Comprehensive (loss) income

 $(2,783) $7,941  $4,583  $22,018 

 

See accompanying notes to Condensed Consolidated Financial Statements.

 

Page 3


 

 

Mesa Laboratories, Inc.

Condensed Consolidated Statements of Cash Flows

(unaudited)

(in thousands)

 

 

Nine Months Ended December 31,

  

Six Months Ended September 30,

 
 

2020

  

2019

  

2021

  

2020

 

Cash flows from operating activities:

          
Net (loss) income $(646) $3,330 

Adjustments to reconcile net (loss) income to net cash provided by operating activities:

     

Net income

 $5,715  $3,896 

Adjustments to reconcile net income to net cash provided by operating activities:

 
Depreciation and amortization 12,933 7,501  8,849 8,333 
Stock-based compensation 6,887 5,310 

Stock-based compensation expense

 4,236  3,276 
Non-cash interest and debt amortization 4,024 2,002  443 2,667 
Amortization of step-up in inventory basis (436) 5,134 
Change in inventory reserve 368 577 
Foreign currency adjustments 4,583 (256)
Other (1,285) 758  (224) 321 

Cash provided by changes in operating assets and liabilities

     

Cash (used in) provided by changes in operating assets and liabilities:

 
Accounts receivable, net 2,224 11  1,065 3,077 
Inventories, net (485) 304  (808) (464)
Prepaid expenses and other assets (2,691) (2,410) (1,473) (1,941)
Accounts payable 71 64  (167) (1,604)
Accrued liabilities and taxes payable (2,517) (4,396) (4,596) (4,811)
Unearned revenues  523  227  983 (140)
Net cash provided by operating activities  23,553  18,156   14,023   12,610 

Cash flows from investing activities:

          
Acquisitions $0 $(184,102)
Purchases of property, plant and equipment  (954)  (935) (1,591) (707)
Net cash (used in) investing activities  (954)  (185,037)  (1,591)  (707)

Cash flows from financing activities:

          
Proceeds from the issuance of convertible senior notes, net 0 167,070 
Proceeds from the issuance of common stock, net 145,935 84,995  0  145,935 
Payments of debt 0 (23,000)
Dividends (2,341) (2,019) (1,658) (1,522)
Payments of Contingent Consideration (11) (11)
Proceeds from the exercise of stock options  3,692  3,848  3,081  2,701 

Payments of contingent consideration

 0 (10)
Net cash provided by financing activities  147,275  230,883   1,423   147,104 
Effect of exchange rate changes on cash and cash equivalents 2,477 (509) 574 1,537 
Net increase in cash and cash equivalents 172,351 63,493  14,429  160,544 

Cash and cash equivalents at beginning of period

  81,380   10,185   263,865   81,380 

Cash and cash equivalents at end of period

 $253,731  $73,678  $278,294  $241,924 

 

See accompanying notes to Condensed Consolidated Financial Statements.

 

Page 4


 

 

Mesa Laboratories, Inc.

Condensed Consolidated Statements of Stockholders’ Equity

(unaudited)

(dollars in thousands, except per share data)

 

 

 

 

Common Stock

          

Common Stock

         
 

Number of Shares

  

Amount

  

Retained Earnings

  

AOCI*

  

Total

  

Number of Shares

  

Amount

  

Retained Earnings

  

AOCI*

  

Total

 

March 31, 2020

 4,387,140  $158,023  $72,359  $(10,369) $220,013 

Proceeds from the issuance of common stock, net of issuance costs of $9,315

 690,000  145,935  -  -  145,935 

March 31, 2021

 5,140,568  $317,652  $72,459  $16,116  $406,227 

Exercise of stock options and vesting of restricted stock units

 25,799  1,654  -  -  1,654  58,324  1,089  0  0  1,089 

Dividends paid, $0.16 per share

 -  -  (704) -  (704)

Dividends paid, $0.16 per share

 -  0  (824) 0  (824)

Stock-based compensation expense

 -  1,268  -  -  1,268  -  2,197  0  0  2,197 

Foreign currency translation

 -  -  -  12,860  12,860  -  0  0  5,371  5,371 

Adoption of accounting standards, net

 -  -  (9) -  (9)

Cumulative adjustment due to adoption of ASU 2020-06

 -  (22,735) 5,683  0  (17,052)

Net income

  -   -   1,217   -   1,217   -   0   1,995   0   1,995 

June 30, 2020

 5,102,939  $306,880  $72,863  $2,491  $382,234 

June 30, 2021

  5,198,892  $298,203  $79,313  $21,487  $399,003 
Exercise of stock options and vesting of restricted stock units 14,502 1,047 - - 1,047  24,340 1,992 0 0 1,992 

Dividends paid, $0.16 per share

 -  -  (818) -  (818)

Dividends paid, $0.16 per share

 - 0 (834) 0 (834)

Stock-based compensation expense

 -  2,008  -  -  2,008  - 2,039 0 0 2,039 

Foreign currency translation

 -  -  -  5,262  5,262  - 0 0 (6,503) (6,503)

Net income

  -   -   2,679   -   2,679   -  0  3,720  0  3,720 

September 30, 2020

 5,117,441  $309,935  $74,724  $7,753  $392,412 
Exercise of stock options and vesting of restricted stock units 13,590 991 0 0 991 
Dividends paid, $0.16 per share - 0 (819) 0 (819)
Stock-based compensation - 3,611 0 0 3,611 
Foreign currency translation - 0 0 21,142 21,142 
Net (loss) income  -  0  (4,542)  0  (4,542)
December 31, 2020  5,131,031 $314,537 $69,363 $28,895 $412,795 

September 30, 2021

  5,223,232 $302,234 $82,199 $14,984 $399,417 

 

 

Common Stock

          

Common Stock

         
 Number of Shares  

Amount

  

Retained Earnings

  

AOCI*

  

Total

  

Number of Shares

  

Amount

  

Retained Earnings

  

AOCI*

  

Total

 

March 31, 2019

 3,890,138  $39,823  $73,303  $(1,815) $111,311 

March 31, 2020

 4,387,140  $158,023  $72,359  $(10,369) $220,013 

Proceeds from the issuance of common stock, net of issuance costs of $9,315

 690,000  145,935  0  0  145,935 

Exercise of stock options and vesting of restricted stock units

 31,441  2,709  -  -  2,709  25,799  1,654  0  0  1,654 

Dividends paid, $0.16 per share

 -  -  (624) -  (624)

Dividends paid, $0.16 per share

 -  0  (704) 0  (704)

Stock-based compensation expense

 -  1,268  0  0  1,268 

Foreign currency translation

 -  0  0  12,860  12,860 

Adoption of accounting standards, net

 -  0  (9) 0  (9)

Net income

  -   0   1,217   0   1,217 

June 30, 2020

 5,102,939 $306,880 $72,863 $2,491 $382,234 

Exercise of stock options and vesting of restricted stock units

 14,502 1,047 0 0 1,047 

Dividends paid, $0.16 per share

 - 0 (818) 0 (818)

Stock-based compensation expense

 -  868  -  -  868  - 2,008 0 0 2,008 

Foreign currency translation

 -  -  -  121  121  - 0 0 5,262 5,262 

Net income

  -   -   4,662   -   4,662   -   0   2,679   0   2,679 

June 30, 2019

 3,921,579  43,400  77,341  (1,694) 119,047 

Exercise of stock options and vesting of restricted stock units

 12,220  798  -  -  798 
Proceeds from issuance of common stock, net of issuance costs of $5,568 431,250 84,995 - - 84,995 
Proceeds from conversion feature of convertible senior notes, due 2025, net of allocated costs and taxes of $8,338 - 22,735 - - 22,735 

Dividends paid, $0.16 per share

 -  -  (697) -  (697)

Stock-based compensation expense

 -  1,182  -  -  1,182 

Foreign currency translation

 -  -  -  (986) (986)

Net income

  -   0   3,172   0   3,172 
September 30, 2019 4,365,049 $153,110 $79,816 $(2,680) $230,246 
Exercise of stock options and vesting of restricted stock units 5,419 341 0 0 341 
Dividends paid, $0.64 per share - 0 (698) 0 (698)
Stock-based compensation - 3,260 0 0 3,260 
Foreign currency translation - 0 0 6,615 6,615 
Net (loss) income  -  0  (4,504)  0  (4,504)
December 31, 2019  4,370,468 $156,711 $74,614 $3,935 $235,260 

September 30, 2020

  5,117,441 $309,935 $74,724 $7,753 $392,412 

 

*Accumulated Other Comprehensive Income (Loss).

 

See accompanying notes to Condensed Consolidated Financial Statements.

 

Page 5


 

Mesa Laboratories, Inc.

Notes to Condensed Consolidated Financial Statements

(unaudited)

(dollar and share amounts in thousands, unless otherwise specified)

 

 

 

Note 1. Description of Business and Summary of Significant Accounting Policies

 

Description of Business

 

In this quarterly report on Form 10-Q, Mesa Laboratories, Inc., a Colorado corporation, together with its subsidiaries is collectively referred to as “we,” “us,” “our,” the “Company” or “Mesa Labs.“Mesa.

 

We are a multinational manufacturer, developer, and seller of life science tools and critical quality control products and services, many of which are sold into niche markets that are driven by regulatory requirements. We have manufacturing operations in North Americathe United States and Europe, and our products are marketed by our sales personnel in North America, Europe, China, Japan,and Asia, and by independent distributors in these areas as well as throughout the rest of the world. We prefer markets in which we can establish a strong presence and achieve high gross margins.

 

As of December 31, 2020September 30, 2021, we managed our operations in 4four reportable segments, or divisions. Our Sterilization and Disinfection Control division manufactures and sells biological, cleaning, and chemical indicators which are used to assess the effectiveness of sterilization and disinfection processes in the hospital, dental, medical device, and pharmaceutical industries. The division also provides testing and laboratory services, mainly to the dental industry. Our Instruments division designs, manufactures, and markets quality control hardware and disposable products utilized in the healthcare, pharmaceutical, food and beverage, medical device, industrial hygiene, and environmental air sampling industries. During the year ended March 31, 2020, we added a new reportable segment: Biopharmaceutical Development as a result of our acquisition of Gyros Protein Technologies Holding AB ("GPT" or the "GPT acquisition"), which is discussed further in Note 12. "Significant Transactions". Our Biopharmaceutical Development division develops, manufactures, and sells automated systems for protein analysis (immunoassays) and peptide synthesis solutions. Immunoassays and peptide synthesis solutions accelerate the discovery, development, and manufacturing of biotherapeutic drugs. Our Instruments division designs, manufactures, and markets quality control hardware and disposable products utilized in the healthcare, pharmaceutical, food and beverage, medical device, industrial hygiene, and environmental air sampling industries. Our Continuous Monitoring division designs, develops, and markets systems which are used to monitor various environmental parameters such as temperature, humidity, and differential pressure to ensure that critical storage and processing conditions are maintained in hospitals, pharmaceutical and medical device manufacturers,manufacturing facilities, blood banks, pharmacies, and laboratory environments. Non-reportable operating segments (including our Cold Chain Packaging division which ceased operations during the year ended March 31, 2020) and unallocated corporate expenses are reported within Corporate and Other.

 

Basis of Presentation

 

The accompanying unaudited Condensed Consolidated Financial Statements have been prepared in accordance with accounting principles generally accepted in the United States (“U.S. GAAP”) for interim financial information and pursuant to the rules and regulations of the Securities and Exchange Commission. In the opinion of management, such unaudited information includes all adjustments, consisting of normal recurring adjustments necessary for a fair presentation of our financial position and results of operations. The results of operations for the interim periods are not necessarily indicative of results that may be achieved for the entire year. The year-end condensed consolidated balance sheetCondensed Consolidated Balance Sheet data was derived from audited financial statements but does not include all disclosures required by accounting principles generally accepted in the United States of America. This quarterly report should be read in conjunction with the consolidated financial statements included in our annual report on Form 10-K for the year ended March 31, 20202021.

Certain prior year amounts have been reclassified in order to conform to the current year presentation.

Our fiscal year ends on March 31. References in this Quarterly Report to a particular “year” or “year-end” mean our fiscal year, references to the first quarter of fiscal year 2022 refer to the period from April 1, 2021 through June 30, 2021, and references to the second quarter of fiscal year 2022 refer to the period from July 1, 2021 through September 30, 2021. References to “fiscal year 2021” refer to the fiscal year ended March 31, 2021, and to “fiscal year 2022” refer to the fiscal year ending March 31, 2022.

 

Risks and Uncertainties

 

The preparation of financial statements requires the use of estimates and assumptions that affect the reported amounts of assets and liabilities at the reporting date and revenues and expenses during the reporting periods. These estimates represent management's judgement about the outcome of future events. The current global business environment continues to be impacted directly and indirectly by the effects of the novel coronavirus ("COVID-19"), and its variations, and it is not possible to accurately predict the future impact of COVID-19. However, we have reviewed the estimates used in preparing the financial statements and have identified the following factors that have a reasonable possibility of being materially affected by the impacts of COVID-19 during the near term: 

 

Estimates regarding the future financial performance of the business used in the impairment tests for goodwill and long-lived assets acquired in a business combination; however, we have identified no triggering events since our impairment analysis was completed during the three monthsquarter ended March 31, 2020;2021; 

Estimates regarding the recoverability of deferred tax assets and estimates regarding cash needs and associated indefinite reinvestment assertions;

Estimates regarding recoverability forof customer receivables;

Estimates of the net realizable value of inventory.

 

Immaterial Error Correction

During the three months ended September 30, 2020, we identified an immaterial error in the design of our Enterprise Resource Planning tool that resulted in a system failure to eliminate intercompany cost of revenues for certain types of transactions. The error resulted in an overstatement of cost of goods sold and an understatement in gross profit for the Continuous Monitoring, Instruments, and Sterilization and Disinfection Control divisions. The issue began during the three months ended June 30, 2019; we have determined that no financial statement prior to April 1, 2019 was misstated as a result of the previously uneliminated balances in cost of revenues. 

In accordance with Staff Accounting Bulletin ("SAB") No.99Materiality, and SAB No.108Considering the Effects of Prior Year Misstatements when Quantifying Misstatements in the Current Year Financial Statements, we evaluated the error quantitatively and qualitatively and determined that the related impact was not material to our financial statements for any prior annual or interim period, but that correcting the cumulative impact of the error would be significant to our results of operations for the three months ended September 30, 2020. In considering the quantitative and qualitative materiality, we concluded that the impact of the error correction is not material in absolute dollar amount especially since our most recent fiscal year results included various new non-cash charges that reduced net income below historical levels. Accordingly, we have revised previously reported financial information for the immaterial error.

Page 6

 

We performed manual intercompany elimination calculations and determined that cost of revenues and accumulated other comprehensive income were overstated by $429 for the year ended March 31, 2020, which would increase operating income and net income by $429 and diluted earnings per share by $0.10; there was no income tax impact on the full year adjustment since the inventory balance was not misstated.  To correct the immaterial error, we have restated retained earnings as of March 31, 2020. The error resulted in overstated cost of goods sold and a corresponding understatement of net income of: $65 during the three months ended June 30, 2019; $110 during the three months ended September 30, 2019, $126 during the three months ended December 31, 2019, and $128 during the three months ended March 31, 2020. Additionally, during the three months ended June 30, 2020, cost of revenues was overstated by $372, which after the impact of taxes would increase net income by $192 and diluted earnings per share by $0.04. We have restated retained earnings as of June 30, 2020 in the amount of $192. The immaterial error has no impact on total cash flows or total comprehensive income for any of the periods that were revised. 

Recently Issued Accounting Pronouncements

 

We have reviewed all recently issued accounting pronouncements and have concluded that they are either not applicable to us or are not expected to have a significant impact on our consolidated financial statements.

Recently Adopted Accounting Pronouncements

In August 2020,the Financial Accounting Standards Board ("FASB") issued Accounting Standards Update ("ASU") No. 2020-06, Debt with Conversion and Other Options and Derivatives and Hedging Accounting for Convertible Instruments and Contracts in an Entity's Own Equity("ASU 2020-06"), which simplifies the accounting for certain financial instruments with characteristics of both liabilities and equity, such as our convertible senior notes, due 2025.2025 (the "Notes"). ASU 2020-06 also enhances transparency and improves disclosures for convertible instruments and earnings per share guidance. It is effective for annual reporting periods beginning after December 15, 2021, including interim periods within those fiscal years. Early adoption is permitted but no earlier thanat the beginning of any fiscal years beginningyear after December 15, 2020. The update permits the use of either the modified retrospective or fullyfull retrospective method of transition.

We intend to adopt theearly adopted ASU2020-06 effective April 1, 2021 but are still evaluating the methodon a modified retrospective basis, and our adoption of this standard had a material effect on our consolidated financial statements. Upon adoption, we derecognized the $22,735 equity conversion feature, net of taxes, that was recorded to common stock, and we derecognized the deferred tax liability of $5,747. We recorded an increase of $22,799 in aggregate to the Note balance as a result of the reversal of the separation of the debt and equity components of the convertible debt. The net effect of these adjustments, which represents $5,683 of historical non-cash interest expense, net of taxes, was recorded as an increase in the balance of beginning retained earnings as of April 1, 2021. The adoption of this standard will utilize. We are continuingsignificantly decrease the amount of non-cash interest expense recognized in future periods as a result of eliminating the discount associated with the equity component. Our statements of cash flows reflect the lower non-cash interest expense in effect after the adoption of ASU 2020-06.

In each period in which the Notes have been outstanding, we have always intended to evaluatesettle the financialNotes in shares of common stock rather than in cash, and therefore, we have applied the if-converted method to calculate the potentially dilutive impact of the Notes on earnings per share. In each reporting period, we have determined that the Notes were antidilutive. Due to decreases in non-cash interest expense that will result from the adoption of ASU 2020-06, on our financial statements but anticipate that subsequent to adoption,it is likely the equity conversion featureNotes will be categorized ashave a liability and there will be a reductiondilutive effect in non-cash interest expense related to the 1.375% convertible senior notes due August 15, 2025 (the "Notes"). Non-cash interest on the equity conversion feature has contributed $3,510 to expense during the nine months ended December 31, 2020, future periods, which would not have been incurred under ASU 2020-06, which we will adopt as of April 1, 2021.

Recently Adopted Accounting Pronouncements

In June 2016, the FASB issued ASU No.2016-13,Financial Instruments -Credit Losses (Topic 326): Measurement of Credit Losses on Financial Instruments, as modified by ASU No.2018-19,Codification Improvements to Topic 326, Financial Instruments - Credit Losses, which amends the impairment model by requiring entities to use a forward-looking approach based on expected losses rather than incurred losses to estimate credit losses on certain types of financial instruments, including trade receivables. The ASU was effective for public business entities for fiscal years beginning after December 15, 2019, with early adoption permitted. On April 1, 2020, we adopted the ASU using the modified retrospective transition method. We recorded a net decrease to beginning retainedour diluted earnings of $9 as of April 1, 2020 due to the cumulative effect of adopting Topic 326's requirement to use a forward-looking approach based on expected losses rather than incurred losses to estimate credit losses on our trade receivables. As a result of the adoption of the ASU, our allowance for doubtful accounts as of December 31, 2020 reflects our best estimate of the expected future losses for our accounts receivable based on current economic conditions. We have accounted for the macroeconomic impact of the COVID-19 pandemic in our estimates, but due to the unprecedented nature of the impact of the pandemic, our estimates may change and future actual losses may differ from current estimates. We will continue to monitor economic conditions and will revise our estimate of expected future losses for accounts receivable as necessary.  

We are exposed to credit losses primarily through sales of products and services. Our expected loss allowance methodology for accounts receivable was developed using historical collection experience, current and expected future economic and market conditions and a review of the current status of customers’ trade accounts receivables. Customers are pooled based on shared specific risk factors. Due to the short-term nature of trade receivables, the estimated accounts receivable that may not be collected is based on the aging of accounts receivable balances.

Customers are assessed for credit worthiness upfront through a credit review. We evaluate contract terms and conditions, and may require prepayment to mitigate risk of loss. Specific allowance amounts are established to record the appropriate provision for customers with a higher probability of default. We monitor changes to the receivables balance on timely basis, and balances are written off as they are determined to be uncollectable after all collection efforts have been exhausted. Estimates of potential credit losses are used to determine the allowance based on assessment of anticipated payment and all other historical, current and future information reasonably available.per share. 

 

 

Note 2. Revenue Recognition

 

We design, manufacture, market, sell, and maintain quality control instruments and software, consumables, and services driven primarily by the regulatory requirements of niche markets. Our consumables, such as biological indicator test strips are typically used on a standalone basis; however, some such consumables used in protein synthesisSales of hardware and calibration solutions are also critical to the ongoing use of our instruments. Hardware and software, sales, such as medical meters, protein synthesizers, wireless sensor systems, and data loggers, are generally driven by our acquisition of new customers, growth of existing customers, or customers' replacement ofcustomers replacing existing equipment. Hardware sales may be offered with accompanying perpetual or annual software licenses, which in some cases are required for the hardware to function. Our Biopharmaceutical Development Division designs, manufactures, markets, and sells instruments, such as protein synthesizers that are used to process immunoassay samples, and related software designed to enhance productivity; consumable chemical solutions designed for use in testing; andWe also offer on-demand and long-termannual service contracts to support customers' use of theour equipment. The division generates revenue from the same general categoriesOur consumables, such as those we have identified for the restbiological indicator test strips, are typically used on a standalone basis; however, some of our businesschemical solutions, such as protein synthesis and recognizes revenue consistently withcalibration solutions, are critical to the ongoing use of our policies.instruments. Consumables are typically used on a one-time basis and require frequent replacement in our customers' operating cycles. We evaluate our revenues internally by product line,based on operating segment, the timing of revenue generation, and the nature of goods and services provided. Typically, discrete revenue is recognized at the shipping point or upon completion of the service, while contracted revenue is recognized over a period of time reflective of the performance obligation period in the applicable contract. Consumables are typically single use items requiring frequent replacement in our customers' operating cycles. Substantially all of our revenues and related receivables are generated from contracts with customers that are 12 months or less in duration.

 

Page 7

 

 

The following tables present disaggregated revenues for the three and ninesix months ended December 31, 2020September 30, 2021 and three and nine months ended December 31, 20192020, respectively:

 

 

Three Months Ended December 31, 2020

  

Three Months Ended September 30, 2021

 
 

Sterilization and Disinfection Control

  

Instruments

  

Biopharmaceutical Development

  

Continuous Monitoring

  

Corporate and Other

  

Total

  

Sterilization and Disinfection Control

  

Biopharmaceutical Development

  

Instruments

  

Continuous Monitoring

  

Total

 

Discrete Revenues

              
Consumables $11,250 $717 $3,406 $9 $0 $15,382  $11,985  $5,218  $853  $7  $18,063 

Hardware and Software

 151  6,210  3,771  1,920  0  12,052  85  3,472  4,485  2,063  10,105 

Services

 433  2,042  506  799  0  3,780  493  850  1,632  1,349  4,324 

Contracted Revenues

              

Services

  1,243   2   1,028   685   0   2,958 

Services and Software

  1,470   1,015   0   863   3,348 

Total Revenues

 $13,077  $8,971  $8,711  $3,413  $0  $34,172  $14,033  $10,555  $6,970  $4,282  $35,840 

 

 

Three Months Ended December 31, 2019

  

Three Months Ended September 30, 2020

 
 

Sterilization and Disinfection Control

  

Instruments

  

Biopharmaceutical Development

  

Continuous Monitoring

  

Corporate and Other

  

Total

  

Sterilization and Disinfection Control

  

Biopharmaceutical Development

  

Instruments

  

Continuous Monitoring

  

Total

 

Discrete Revenues

              
Consumables $9,948 $781 $1,941 $13 $229 $12,912  $9,518  $3,238  $715  $15  $13,486 

Hardware and Software

 95  6,881  2,571  2,562  0  12,109  108  4,191  4,815  2,207  11,321 

Services

 360  2,352  656  849  0  4,217  706  1,005  2,028  614  4,353 

Contracted Revenues

              

Services

  1,216   0   469   732   0   2,417 

Services and Software

  1,220   697   0   783   2,700 

Total Revenues

 $11,619  $10,014  $5,637  $4,156  $229  $31,655  $11,552  $9,131  $7,558  $3,619  $31,860 

 

 

Nine Months Ended December 31, 2020

  

Six Months Ended September 30, 2021

 
 

Sterilization and Disinfection Control

  

Instruments

  

Biopharmaceutical Development

  

Continuous Monitoring

  

Corporate and Other

  

Total

  

Sterilization and Disinfection Control

  

Biopharmaceutical Development

  

Instruments

  

Continuous Monitoring

  

Total

 

Discrete Revenues

              
Consumables $32,252 $2,240 $8,583 $54 $0 $43,129  $24,861  $8,826  $1,795  $17  $35,499 

Hardware and Software

 388  16,045  10,518  6,082  0  33,033  245  7,029  9,723  3,907  20,904 

Services

 1,389  5,922  2,293  1,944  0  11,548  1,194  1,432  3,014  2,202  7,842 

Contracted Revenues

              

Services

  3,667   2   2,397   2,197   0   8,263 

Services and Software

  2,883   2,145   0   1,487   6,515 

Total Revenues

 $37,696  $24,209  $23,791  $10,277  $0  $95,973  $29,183  $19,432  $14,532  $7,613  $70,760 

 

 

Nine Months Ended December 31, 2019

  

Six Months Ended September 30, 2020

 
 

Sterilization and Disinfection Control

  

Instruments

  

Biopharmaceutical Development

  

Continuous Monitoring

  

Corporate and Other

  

Total

  

Sterilization and Disinfection Control

  

Biopharmaceutical Development

  

Instruments

  

Continuous Monitoring

  

Total

 

Discrete Revenues

              
Consumables $30,487 $2,364 $1,941 $34 $2,415 $37,241  $21,002  $5,177  $1,523  $45  $27,747 

Hardware and Software

 429  19,282  2,571  6,374  0  28,656  237  6,747  9,835  4,162  20,981 

Services

 1,301  6,872  656  1,959  27  10,815  956  1,787  3,880  1,145  7,768 

Contracted Revenues

              

Services

  3,606   0   469   2,692   0   6,767 

Services and Software

  2,424   1,369   0   1,512   5,305 

Total Revenues

 $35,823  $28,518  $5,637  $11,059  $2,442  $83,479  $24,619  $15,080  $15,238  $6,864  $61,801 

 

Page 8

 

Revenues from external customers are attributed to individual countries based upon the locations to which the products are shipped or exported, as follows:

 

 

Three Months Ended December 31,

  

Nine Months Ended December 31,

  

Three Months Ended September

  

Six Months Ended September 30,

 
 

2020

  

2019

  

2020

  

2019

  

2021

  

2020

  

2021

  

2020

 

United States

 $18,480  $17,810  $52,246  $48,007  $19,384  $11,222  $37,839  $27,594 

Foreign

  15,692   13,845   43,727   35,472   16,456   20,638   32,921   34,207 

Total revenues

 $34,172  $31,655  $95,973  $83,479  $35,840  $31,860  $70,760  $61,801 

 

No foreign country exceeds 10% of total revenues.

 

Contract Balances

Our contracts have varying payment terms and conditions. Some customers prepay for products and services, resulting in unearned revenues or customer deposits, called contract liabilities, which are included within other accrued expenses and unearned revenues in the accompanying Condensed Consolidated Balance Sheets. Contract assets would exist when sales are recorded (i.e. the control of the goods or services has been transferred to the customer), but customer payment is contingent on a future event besides the passage of time (such as satisfaction of additional performance obligations). We dodid not have any contract assets. assets as of September 30, 2021 or March 31, 2021. Unbilled receivables, which are not classified as contract assets, represent arrangements in which sales have been recorded prior to billing and right to payment is unconditional.

 

A summary of contract liabilities is as follows:

 

Contract liabilities balance as of March 31, 2020

$7,217 

Prior year liabilities recognized in revenues during the nine months ended December 31, 2020

 (4,131)

Contract liabilities added during the nine months ended December 31, 2020, net of revenues recognized

 4,984 

Contract liabilities balance as of December 31, 2020

$8,070 

Contract liabilities as of March 31, 2021

 $8,994 

Prior year liabilities recognized in revenues during the six months ended September 30, 2021

  (3,910)

Contract liabilities added during the six months ended September 30, 2021, net of revenues recognized

  5,592 

Contract liabilities balance as of September 30, 2021

 $10,676 

 

 

Note 3. Fair Value Measurements

 

Our financial instruments consist primarily of cash and cash equivalents, trade accounts receivable, obligations under trade accounts payable, and debt. Due to their short-term nature, the carrying values for cash and cash equivalents, trade accounts receivable, and trade accounts payable approximate fair value. We measure our cash equivalents at fair value using quoted market prices in an active market, and we classify them within Level 1 of the fair value hierarchy, and we value them using quoted market prices in an active market.  As of December 31, 2020 and March 31, 2020, cashhierarchy. Cash and cash equivalents on our Condensed Consolidated Balance Sheets included $222,819$240,822 and $66,735, respectively,$230,822 in a money market account. The increase in the balance in our money market account is primarily a resultas of our public offering of common stock described in further detail in Note 8.September 30, 2021 "Stockholders' Equity". and March 31, 2021, respectively.

 

During thefiscal year ended March 31, 2020,, we issued $172,500 aggregate principal of 1.375% convertible senior notes due August 15, 2025. We estimate the fair value of the Notes based on Level 2 inputs of the last actively traded price or market observable input before the end of the reporting period. The estimated fair value and carrying value of the Notes are as follows:

 

  

December 31, 2020

  

March 31, 2020

 
  

Carrying Value

  

Fair Value (Level 2)

  

Carrying Value

  

Fair Value (Level 2)

 

Notes

 $144,302  $206,569  $140,278  $173,363 
  

September 30, 2021

  

March 31, 2021

 
  

Carrying Value

  

Fair Value (Level 2)

  

Carrying Value

  

Fair Value (Level 2)

 

Notes

 $168,917  $211,097  $145,675  $188,780 

 

The carrying value of the Notes areincreased as a result of the adoption of ASU 2020-06, discussed in more detailfurther in Note 7.1. "Description of Business and Summary of Significant Accounting Policies" and Note 6. "Indebtedness." 

 

Assets recognized or disclosed at fair value in the unaudited condensed consolidated financial statements on a nonrecurring basis include items such as property and equipment, operating lease assets, goodwill, and other intangible assets, including those that were part of the GPT Acquisition.assets. These assets are measured at fair value if determined to be impaired. The fair values assigned to the assets and liabilities acquired in the GPT Acquisition were measured using Level 3 inputs, as discussed further in Note 12. "Significant Transactions." There were no transfers between the levels of the fair value hierarchy during the ninethree and six months ended December 31, 2020September 30, 2021 or the ninethree and six months ended December 31, 2019September 30, 2020.

 

Cash and cash equivalents and accounts receivables are the financial instruments that subject us to the highest concentration of credit risk. It is our policy to invest cash equivalents in highly liquid cash equivalent financial instruments with high credit ratings, and low exposure to anymaintain low single issuer exposure (except U.S. treasuries). Concentration of credit risk with respect to accounts receivable is limited to customers to whom we make significant sales. We reserve an allowance for potential write-offs of accounts receivable using historical collection experience and current and expected future economic and market conditions, but we have not written off any significant accounts to date. To controlmanage credit risk, we perform regular credit evaluationsconsider the creditworthiness of our customers’ financial condition. new and existing customers, and we regularly review outstanding balances and payment histories. We may require pre-payments from customers under certain circumstances and may limit future purchases until payments are made on past due amounts.

 

 

Note 4. Inventories, Net

 

Inventories consist of the following:

 

 

December 31, 2020

  

March 31, 2020

  

September 30, 2021

  

March 31, 2021

 

Raw materials

 $8,151  $6,757  $7,610  $5,755 

Work-in-process

 436  329 

Work in process

 423  426 

Finished goods

 6,370  9,768  4,084  4,997 

Less: reserve

  (2,992)  (2,624)

Inventories, net

 $11,965  $14,230  $12,117  $11,178 

 

The remaining balance of the adjustment to step upRaw materials inventory to fair value as part of the GPT Acquisition, which was included in finished goods, was $0 and $2,901, respectively,higher as of December 31, 2020September 30, 2021 andcompared to March 31, 20202021, ; see Noteprimarily because we ordered higher than usual quantities of some components during the 12.second "Significant Transactions."quarter of fiscal year 2022 to mitigate supply chain risks. 

 

Page 9

 

Note 5. Goodwill and Intangible Assets, Net

 

Finite-lived intangible assets consist of the following:

 

 

December 31, 2020

  

March 31, 2020

  

September 30, 2021

  

March 31, 2021

 
 

Gross Carrying Amount

  

Accumulated Amortization

  

Net Carrying Amount

  

Gross Carrying Amount

  

Accumulated Amortization

  

Net Carrying Amount

  

Gross Carrying Amount

  

Accumulated Amortization

  

Net Carrying Amount

  

Gross Carrying Amount

  

Accumulated Amortization

  

Net Carrying Amount

 

Intellectual property

 $21,909  $(8,262) $13,647  $15,731  $(6,454) $9,277  $21,094  $(9,409) $11,685  $21,201  $(8,595) $12,606 

Trade names

 8,875  (3,060) 5,815  5,839  (2,855) 2,984  8,574  (3,265) 5,309  8,612  (3,129) 5,483 

Customer relationships

 151,027  (49,800) 101,227  146,106  (38,777) 107,329  144,869  (58,459) 86,410  145,754  (52,206) 93,548 

Non-compete agreements

  1,299   (1,185)  114   1,447   (1,166)  281   1,299   (1,215)  84   1,299   (1,195)  104 

Total

 $183,110  $(62,307) $120,803  $169,123  $(49,252) $119,871  $175,836  $(72,348) $103,488  $176,866  $(65,125) $111,741 

 

The increase in the carrying amount of intangible assets was attributable to changes in foreign currency and adjustments to the preliminary purchase price of GPT that are discussed further in Note 12. "Significant Transactions". Amortization expense for finite-lived intangible assets acquired in a business combination was $3,828$3,757 and $10,694$7,573 for the three and ninesix months ended December 31, 2020September 30, 2021, respectively, and $2,565$3,512 and $5,895$6,866 for the three and ninesix months ended December 31, 2019September 30, 2020, respectively. The increase in amortization expense was attributable to intangible assets acquired as part ofDuring the GPT acquisition, including a cumulative effect true up recorded during the three monthsquarter ended June 30, 2020, as we made adjustmentsreduced the value of our intangible assets due to a purchase accounting, see Note 12. "Significant Transactions."price adjustment that resulted in a cumulative effect net decrease to amortization expense of $334. 

 

TheFor the following is estimated amortization expense for thefiscal years ending March 31:31, amortization expense is estimated as follows:

 

Remainder of year ending March 31, 2021

 $3,891 

2022

 15,470 

Remainder of 2022

 7,398 

2023

 15,261  14,622 

2024

 14,746  14,107 

2025

 13,143  12,515 

2026

 11,731 

 

The change in the carrying amount of goodwill was as follows:

 

  

Sterilization and Disinfection Control

  

Instruments

  

Biopharmaceutical Development

  

Continuous Monitoring

  

Corporate and Other

  

Total

 

March 31, 2020

 $29,594  $19,123  $74,716  $18,103  $0  $141,536 

Effect of foreign currency translation

  894   106   16,183   0   0   17,183 

Goodwill adjustment related to GPT acquisition

  0   0   7,065   0   0   7,065 

December 31, 2020

 $30,488  $19,229  $97,964  $18,103  $0  $165,784 
  

Sterilization and Disinfection Control

  

Biopharmaceutical Development

  

Instruments

  

Continuous Monitoring

  

Total

 

March 31, 2021

 $30,153  $93,399  $19,186  $18,103  $160,841 

Effect of foreign currency translation

  (100)  (752)  (12)  0   (864)

September 30, 2021

 $30,053  $92,647  $19,174  $18,103  $159,977 

 

 

Note 6.6 Supplemental Balance Sheets Information. Indebtedness

 

Accrued payrollCredit Facility

On March 5, 2021, we entered into a four-year senior secured credit agreement that includes 1) a revolving credit facility in an aggregate principal amount of up to $75,000, 2) a swingline loan in an aggregate principal amount not exceeding $5,000, and benefits consist3) letters of credit in an aggregate stated amount not exceeding $2,500 at any time. The Credit Facility also provides for an incremental term loan or an increase in revolving commitments in an aggregate principal amount of at a minimum $25,000 and at a maximum $75,000, subject to the satisfaction of certain conditions and lender considerations (together, the available facilities are referred to as the "Credit Facility").

The Credit Facility bears interest at either a base rate or a Eurodollar rate, plus an applicable spread. The balance of unamortized customary lender fees was $567 and $650 as of September 30, 2021 and March 31, 2021, respectively. On our Consolidated Balance Sheets, the short term portion is recorded within prepaid expenses and other, and the long term portion is recorded in other assets. The fees are being expensed on a straight line basis over the life of the following:agreement. 

 

  

December 31, 2020

  

March 31, 2020

 

Bonus payable

 $2,796  $4,069 

Wages payable

  2,746   2,485 

Payroll related taxes

  1,478   2,228 

Other benefits payable

  168   158 

Total accrued payroll and benefits

 $7,188  $8,940 

The most restrictive financial covenants include a maximum leverage ratio of 5.50 to 1.00 for the firstfour testing dates on which the line of credit is outstanding; 5.0 to 1.0 on each of the fifth, sixth, seventh, and eighth testing dates; and 4.5 to 1.0 on each testing date following the eighth testing date, except that we may have a leverage ratio of 5.75 to 1.0 for a period of four consecutive quarters following a permitted acquisition. The Credit Facility also stipulates a minimum fixed charge coverage ratio of 1.25 to 1.0. Other covenants include restrictions on our ability to incur debt, grant liens, make fundamental changes, engage in certain transactions with affiliates, or conduct asset sales. As of September 30, 2021, we were in compliance with all required covenants.

 

Other accrued expenses consistAs of and throughout the three and six months ended September 30, 2021, we had 0 outstanding balance under the Credit Facility. On October 18, 2021, we drew $70,000 under our line of credit to provide a portion of the following:cash needed to complete the acquisition of Agena Biosciences, Inc. ("Agena") as further discussed in Note 11. "Significant Transactions." We are obligated to pay quarterly unused commitment fees of between 0.15% and 0.35% of the Credit Facility’s aggregate principal amount, based on our leverage ratio. Since the Credit Facility's inception, the rate applied to our unused commitment fees has been 0.15%. We incurred unused commitment fees of $28 and $57 during the three and six months ended September 30, 2021, respectively, and $0 and $0 during the three and six months ended September 30, 2020, respectively.

  

December 31, 2020

  

March 31, 2020

 

Accrued business taxes

 $4,798  $3,796 

Current operating lease liabilities

  1,057   1,095 

Interest payable

  889   296 

Professional services fees

  404   857 
Contingent consideration  555   504 

Other

  1,462   298 

Total other accrued expenses

 $9,165  $6,846 

 

Page 10

 

Note 7. Indebtedness

Convertible Notes 

On August 12, 2019, we issued an aggregate principal amount of $172,500 of convertible senior notes (the "Notes").notes. The Notes mature on August 15, 2025, unless earlier repurchased or converted, and bear interest at a rate of 1.375% payable semi-annually in arrears on February 15 and August 15 each year beginning on February 15, 2020. The Notes are initially convertible at a conversion rate of 3.5273 shares of the common stock per $1,000 principal amount of Notes, which is equivalent to an initial conversion price of approximately $283.50 per share of common stock. Noteholders may convert their Notes at their option only in the following circumstances: (i) during any calendar quarter commencing after the calendar quarter ended on December 31,2019 (and only during such calendar quarter), if the last reported sale price per share of  our common stock exceeds 130% of the conversion price for each of at least 20 trading days during the 30 consecutive trading days ending on, and including, the last trading day of the immediately preceding calendar quarter; (ii) during the five consecutive business days immediately after any 10 consecutive trading day period (such 10 consecutive trading day period, the “measurement period”) in which the trading price per $1,000 principal amount of Notes for each trading day of the measurement period was less than 98% of the product of the last reported sale price per share of our common stock on such trading day and the conversion rate on such trading day; (iii) upon the occurrence of certain corporate events or distributions on our common stock, including certain distributions, the occurrence of a fundamental change (as defined in the indenture governing the Notes) or a transaction resulting in the Company’s common stock converting into other securities or property or assets; and (iv) 

(i)during any calendar quarter commencing after the calendar quarter ended on December 31,2019 (and only during such calendar quarter), if the last reported sale price per share of our common stock exceeds 130% of the conversion price for each of at least 20 trading days during the 30 consecutive trading days ending on, and including, the last trading day of the immediately preceding calendar quarter;
(ii)during the five consecutive business days immediately after any 10 consecutive trading day period (such 10 consecutive trading day period, the “measurement period”) in which the trading price per $1,000 principal amount of Notes for each trading day of the measurement period was less than 98% of the product of the last reported sale price per share of our common stock on such trading day and the conversion rate on such trading day;
(iii)upon the occurrence of certain corporate events or distributions on our common stock, including certain distributions, the occurrence of a fundamental change (as defined in the indenture governing the Notes) or a transaction resulting in the Company’s common stock converting into other securities or property or assets; and
(iv)at any time from, and including, April 15, 2025 until the close of business on the second scheduled trading day immediately before the maturity date. 

Upon conversion, we will pay or deliver, as the case may be, cash, shares of our common stock, or a combination of cash and shares of our common stock, at our election. Our current intent is to settle conversions entirely in shares of common stock. We will reevaluate this policy from time to time as we receive conversion notices are received from holders of the Notes.note holders. The circumstances required to allow the holders to convert their Notesnecessary for conversion were not met during the three or sixmonths ended December 31, 2020September 30, 2021. As of December 31, 2020September 30, 2021, the Notes are classified as a long-term liability on our Condensed Consolidated Balance Sheets as the circumstances necessary for conversion were not satisfied as of the end of the period. The if-converted value of the Notes exceededdid not exceed the principal balance.balance as of September 30, 2021.

 

We accounted for the transaction by bifurcatingDebt issuance costs related to the Notes into liabilityare comprised of discounts and equity components.commissions payable to the initial purchasers of $5,175 and third party offering costs of $255. The carrying amount of the liability component was $141,427 upon issuance as calculated using the income approach and measuring the fair value of a similar debt instrument that does not have an associated convertible feature. The implied interest rate (a Level 3 unobservable input) assuming no conversion option was estimated using the Tsiveriotis-Fernandes model; all other assumptions used in measuring the fair value represent inputs market participants would use in pricing the liability component, including market interest rates, credit standing, and yield curves, all of which are defined as Level 2 observable inputs before allocated issuance costs and deferred taxes.  The carrying amount of the equity component representing the conversion option was $31,073 and was determined by deducting the fair value of the liability component from the par value of the Notes. The equity component is not remeasured as long as it continues to meet the conditions for equity classification. The excess of the principal amount of the liability component over its carrying amount (the "Debt Discount") isare being amortized to interest expense using the effective interest method over the six-year contractual term of the Notes.

 

DebtDue to our adoption of ASU 2020-06 on April 1, 2021, we no longer bifurcate the Notes into a liability and an equity component in our Condensed Consolidated Balance Sheets (see Note 1. "Description of Business and Summary of Significant Accounting Policies"). The Notes are accounted for entirely as a liability, and the issuance costs related to the Notes comprised of discounts and commissions payable to the initial purchasers of $5,175 and third party offering costs of $255. We allocated the total amount incurred to the liability and equity components of the Notes based on their relative values. Issuance costsare accounted for wholly as debt issuance costs. The equity conversion feature that was recorded to common stock, as well as the unamortized debt discount and amortization expense attributable to the liability component were $4,452 and are being amortized to interest expense using the effective interest method over the contractual term.  Issuance costs attributable to the equity, component were netted with the equity component in stockholders’ equity.have been derecognized.

 

The net carrying amount of the Notes werewas as follows:

 

  

December 31, 2020

  

March 31, 2020

 

Principal outstanding

 $172,500  $172,500 

Unamortized debt discount

  (24,696)  (28,205)

Unamortized debt issuance costs

  (3,502)  (4,017)

Net carrying value

 $144,302  $140,278 

The net carrying amount of the equity component of the Notes were as follows:

  

December 31, 2020

  

March 31, 2020

 

Amount allocated to conversion option

 $31,073  $31,073 

Less: allocated issuance costs and deferred taxes

  (8,338)  (8,338)

Equity component, net

 $22,735  $22,735 
  

September 30, 2021

  

March 31, 2021

 

Principal outstanding

 $172,500  $172,500 

Unamortized debt discount attributable to equity

  0   (23,497)

Unamortized debt issuance costs

  (3,583)  (3,328)

Net carrying value

 $168,917  $145,675 

 

We recognized interest expense on the Notes as follows:

 

 

Three Months Ended December 31,

  

Nine Months Ended December 31,

  

Three Months Ended September 30,

  

Six Months Ended September 30,

 
 

2020

  

2019

  

2020

  

2019

  

2021

  

2020

  

2021

  

2020

 

Coupon interest expense at 1.375%

 $593  $593  $1,779  $909  $593  $593  $1,186  $1,186 

Amortization of debt discounts and issuance costs

  1,357   1,295   4,024   2,002   222   1,341   443   2,667 

Total

 $1,950  $1,888  $5,803  $2,911  $815  $1,934  $1,629  $3,853 

 

The effective interest rate ofon the liability component of the notenotes is approximately 1.9%. Prior to the adoption of ASU 2020-06, the effective interest rate was approximately 5.5%.

 

Page 11

 

Note 87. Stockholders' Equity

 

Public Offerings of Common Stock

On June 12, 2020, we completed the sale and issuance of 600,000 shares of our common stock and on June 19, 2020, our underwriters exercised in full their option to purchase an additional 90,000 shares of our common stock. The offering price to the public was $225.00 per share. The total proceeds we received from the offering, net of underwriting discounts and commissions and other offering expenses was $145,935. 

Stock-Based Compensation

During the three months ended September 30, 2021, our shareholders approved the Mesa Laboratories, Inc. 2021 Equity Incentive Plan (the "2021 Equity Plan"), which authorizes the issuance of 330 shares of common stock to eligible participants. For the purpose of counting the shares remaining under the 2021 Equity Plan, each share underlying a stock option or a full value award (such as restricted stock units and performance shares) counts as one share used. The 2021 Equity Plan is administered by the Compensation Committee of the Board of Directors, which has the authority to grant equity awards, or to delegate its authority under the plan to make grants (subject to certain legal and regulatory restrictions), including the authority to determine the individuals to whom awards will be granted, the type of awards and when the awards are to be granted, the number of shares to be covered by each award, the vesting schedule, and all other terms and conditions of the awards.

Our 2021 Equity Plan includes retiree provisions, which result in the acceleration of stock-based compensation expense for retiree-eligible participants. 

Page 11

The exercise price for stock awards granted under the 2021 Equity Plan cannot be less than fair market value at the date of grant. Shares issued during the six months ended September 30, 2021 were issued in connection with the 2021 Equity Plan.

Amounts recognized related to stock-based compensation are as follows: 

 

 

Three Months Ended December 31,

  

Nine Months Ended December 31,

  

Three Months Ended September 30,

  

Six Months Ended September 30,

 
 

2020

  

2019

  

2020

  

2019

  

2022

  

2021

  

2021

  

2020

 

Stock-based compensation expense

 $3,611  $3,260  $6,887  $5,310  $2,039  $2,008  $4,236  $3,276 

Amount of income tax expense (benefit) recognized in earnings

  320   (78)  (1,127)  (986)

Amount of income tax (benefit) recognized in earnings

  (719)  (522)  (3,504)  (1,447)

Stock-based compensation expense, net of tax

 $3,931  $3,182  $5,760  $4,324  $1,320  $1,486  $732  $1,829 

 

Stock-based compensation expense is included in cost of revenues, selling, general and administrative, and research and development expense in the accompanying unaudited Condensed Consolidated Statements of Operations.Income.

 

The following is a summary of stock option award activity for the ninesix months ended December 31, 2020September 30, 2021: (shares in thousands):

 

  

Stock Options

 
  

Shares Subject to Options

  

Weighted- Average Exercise Price per Share

 

Outstanding at March 31, 2020

  286  $107.72 

Awards granted

  36   226.72 

Awards forfeited or expired

  (12)  116.24 

Awards exercised

  (47)  85.64 

Outstanding as of December 31, 2020

  263  $127.63 
 
  

Stock Options

 
  

Shares Subject to Options

  

Weighted- Average Exercise Price per Share

  

Weighted-Average Remaining Contractual Life (Years)

  

Aggregate Intrinsic Value

 

Outstanding as of March 31, 2021

  253  $129.55   2.7  $28,856 

Awards granted

  37   268.85         

Awards forfeited or expired

  (3)  173.29         

Awards exercised

  (37)  94.49         

Outstanding as of September 30, 2021

  250  $154.16   2.9  $37,092 

The stock options granted during the ninesix months ended December 31, 2020September 30, 2021 vest in equal installments on each of the firstSeptember 1, 2022, threeJune 15, 2023 anniversaries of the grant date. and June 15, 2024.

 

The following is a summary of restricted stock unit ("RSU") award activity for the ninesix months ended December 31, 2020September 30, 2021: (shares in thousands): 

 

  

Time-Based Restricted Stock Units

  

Performance-Based Restricted Stock Units

 
  

Number of Shares

  

Weighted- Average Grant Date Fair Value per Share

  

Number of Shares

  

Weighted- Average Grant Date Fair Value per Share

 

Nonvested at March 31, 2020

  28  $180.15   22  $204.68 

Awards granted

  21   230.36   0   0 

Awards forfeited or expired

  (3)  204.40   (1)  199.50 

Awards distributed

  (8)  196.38   0   0 

Nonvested as of December 31, 2020

  38  $203.29   21  $204.80 
  

Time-Based Restricted Stock Units

  

Performance-Based Restricted Stock Units

 
  

Number of Shares

  

Weighted- Average Grant Date Fair Value per Share

  

Number of Shares

  

Weighted- Average Grant Date Fair Value per Share

 

Outstanding as of March 31, 2021(1)

  37  $206.56   20  $207.88 

Awards granted

  29   267.09   0   0 

Performance adjustment(2)

  0   0   16   190.07 

Awards forfeited

  (1)  210.22   0   0 

Awards distributed

  (19)  208.13   (28)  197.81 

Outstanding as of September 30, 2021(1)

  46  $244.45   8  $202.00 

(1)

Balances for performance-based restricted stock units ("PSUs") are reflected at target.

(2)

During the three months ended June 30, 2021, the fiscal year 2019 PSUs vested and were paid at 280% of target, based on actual performance results and completion of service conditions. In addition, the PSUs granted to employees of Gyros Protein Technologies Holding AB vested at 60% of target, following a modification of the performance targets by the Compensation Committee of the Board of Directors during fiscal year 2021.

 

The majority of theoutstanding time-based RSUs granted during the nine months ended December 31, 2020 vest and settle in shares of our common stock on a one-for-one basis,basis. The substantial majority of the RSUs granted during the six months ended September 30, 2021 vest in equal installments on each of the firstSeptember 1, 2022, threeJune 15, 2023 anniversaries of the grant date. Time-basedand June 15, 2024, except time-based RSUs issued to non-employee directors, and a portion of the awards granted to executives of the companywhich vest after a one-year period year from the grant date. We recognize the expense relating to RSUs, net of estimated forfeitures, on a straight-line basis over the vesting period.

 

Page 12

Performance-based RSUs vest upon completion of the service period described in the award agreement and based on achievementsachievement of the financial targets described in the award agreements. We recognize the expense relating to the performance-based RSUs based on the probable outcome of achievement of the financial targets on a straight-line basis over the service period. During fiscal year 2020, we awarded 8 PSUs (the "FY 20 PSUs") that are subject to both service and performance conditions to eligible employees. The FY 20 PSUs had a grant date fair value of $202.00 per share and vest based on our achievement of specific performance criteria for the three-year period from April 1, 2019 through March 31, 2022 and on a pro-rata basis after 12 months of continued service through June 15, 2022. The quantity of shares that will be issued upon vesting will range from 0% to 200% of the targeted number of shares; if the defined minimum targets are not met, then no shares will vest. Based on actual and projected performance through the quarter ended September 30, 2021, we estimate that 6 FY 20 PSUs will vest. 

 

During the three months ended December 31, 2020,June 30, 2021, we adjustedthe Compensation Committee of the Board of Directors modified a time-based restricted stock award granted to our estimateChief Executive Officer during fiscal year 2017, distributing 3 remaining outstanding shares effective June 8, 2021. The original award required vesting of performance share units expected to vest, based1 awards on actual results achieved.each: March 20, 2022, 2023, and 2024. As a result of the modification, we recorded a cumulative effect catch uprecognized the previously unrecognized compensation cost of $1,629$351 during the period ($1,209 net of tax as well as $0.25 per basic and diluted share for the ninethree months ended December 31,June 30,2021.

Public Offering of Common Stock

On June 12, 2020, respectively), which is recordedwe completed the sale and issuance of 600 shares of our common stock and on June 19, 2020, our underwriters exercised in general and administrative costs onfull their option to purchase an additional 90 shares of our condensed consolidated statements of operations. During the quarter ending March 31, 2021, we expect non-cash stock based compensation expense will increase approximately $194 comparedcommon stock. The offering price to the quarters ended June 30, 2020 public was $225.00 per share. The total proceeds we received from the offering, net of underwriting discounts and September 30, 2020 as a result of our new estimate of performance share units expected to vest.commissions and other offering expenses was $145,935. 

 

Page 12

 

Note 98. (Loss) Earnings Per Share

 

Basic (loss) earnings per share is computed by dividing net (loss) income by the weighted-average number of common shares outstanding during the reporting period. Diluted (loss) earnings per share (“diluted EPS”) is computed similarly to basic (loss) earnings per share, except that it includes the potential dilution that could occur if dilutive securities were exercised. Potentially dilutive securities include common shares related to stock options and RSUs, including RSUs that contain performance conditions which have been achieved as of the reporting period (collectively “stock awards”)., as well as common shares underlying our convertible senior notes. Stock awards are excluded from the calculation of diluted EPS in the event that they are subject to performance conditions that have not yet been achieved or are antidilutive. Diluted EPS considers the impact of potentially dilutive securities except in periods in which there is a loss because the inclusion of the potential common shares would then have an antidilutive effect. There was no dilution in our diluted EPS calculation for the three and nine months ended December 31, 2020 and the three months ended December 31, 2019 because we incurred net losses in those periods and the effect would have been antidilutive.

 

The impact of the assumed conversion of the Notes calculated under the if-converted method was anti-dilutive, and as such, shares underlying the Notes were excluded from the diluted EPS calculation for the three and ninesix months ended December 31, 2020September 30, 2021. 

 

The following table presents a reconciliation of the denominators used in the computation of basic and diluted (loss) earnings per share (shares in thousands):share:

 

  

Three Months Ended December 31,

  

Nine Months Ended December 31,

 
  

2020

  

2019

  

2020

  

2019

 

Net (loss) income available for shareholders

 $(4,542) $(4,504) $(646) $3,330 

Weighted average outstanding shares of common stock

  5,125   4,367   4,922   4,142 

Dilutive effect of stock options

  0   0   0   251 

Dilutive effect of time-based non-vested shares

  0   0   0   25 

Dilutive effect of performance-based non-vested shares

  0   0   0   0 

Fully diluted shares

  5,125   4,367   4,922   4,418 
                 

Basic (loss) earnings per share

 $(0.89) $(1.03) $(0.13) $0.80 

Diluted (loss) earnings per share

 $(0.89) $(1.03) $(0.13) $0.75 
  

Three Months Ended September 30,

  

Six Months Ended September 30,

 
  

2021

  

2020

  

2021

  

2020

 

Net income available for shareholders

 $3,720  $2,679  $5,715  $3,896 

Weighted average outstanding shares of common stock

  5,211   5,110   5,182   4,821 

Dilutive effect of stock options

  109   119   109   125 

Dilutive effect of RSUs

  24   12   33   12 

Fully diluted shares

  5,344   5,241   5,324   4,958 
                 

Basic earnings per share

 $0.71  $0.52  $1.10  $0.81 

Diluted earnings per share

 $0.70  $0.51  $1.07  $0.79 

 

The following stock awards were excluded from the calculation of diluted EPS:

 

 

Three Months Ended December 31,

  

Nine Months Ended December 31,

  

Three Months Ended September 30,

  

Six Months Ended September 30,

 
 

2020

  

2019

  

2020

  

2019

  

2021

  

2020

  

2021

  

2020

 

Assumed conversion of convertible debt

 608  608  608  318  608  608  608  608 

Stock awards that were anti-dilutive

 307  343  313  22  43  63  40  49 

Stock awards subject to performance conditions

  11   21   17   15   8   21   8   19 

Total stock awards excluded from diluted EPS

  926   972   938   355   659   692   656   676 

 

 

Note 109. Income Taxes

 

For interim income tax reporting, we estimate our annual effective tax rate and apply this effective tax rate to our year-to-date pre-tax income. Each quarter, our estimate of the annual effective tax rate is updated, and if the estimated effective tax rate changes, a cumulative adjustment is made. Additionally, the tax effects of significant unusual or infrequently occurring items are recognized as discrete items in the interim period in which the events occur. The impact of changes in tax laws or rates on deferred tax amounts, impairments of non-deductible goodwill, excess benefits from stock-based compensation, and changes in tax reserves resulting from the finalization of tax audits or reviews are examples of significant unusual or infrequently occurring items that are recognized as discrete items in the interim period in which the event occurs. There is a potential for volatility of the effective tax rate due to several factors, including changes in the mix of the pre-tax income and the jurisdictions to which it relates, changes in tax laws and foreign tax holidays, settlement with taxing authorities, and foreign currency fluctuations.

 

Page 13

Our effective income tax rate was 20.7% and 75.0%4.1% for the three and ninesix months ended December 31, 2020September 30, 2021 and 11.3% and 19.2%(24.2)% for the three and ninesix months ended December 31, 2019September 30, 2020. , respectively.  The effective tax rate for the three and ninesix months ended December 31, 2020September 30, 2021 differed from the statutory federal rate of 21% primarily due to the release of an uncertain tax position during the nine months ended December 31, 2020 as discussed further below, the benefit of share-based payment awards for employees and research and development tax credits,foreign derived intangible income, partially offset by expenses for state income taxes, the limitations imposed by Section 162(m), and the foreign rate differential.

As part of our adoption of the Tax Cuts and Jobs Act, we recorded an uncertain tax position in the amount of $630. During the nine months ended December 31, 2020, the Internal Revenue Service ("IRS") issued final regulations clarifying the law and providing greater flexibility to companies regarding substantiation requirements. As a result of the clarifications, we have determined that the uncertain tax position is no longer required and we have released it, which resulted in a $630 tax benefit during the nine months ended December 31, 2020.expenses for state income taxes.

 

The tax year ended December 31, 2018 for Gyros US, Inc., and its subsidiary, which we acquired as part of the GPT Acquisition,Gyros Protein Technologies ("GPT") acquisition, is under examination by the IRS. Additionally, the tax year ended March 31, 2019for Mesa Laboratories, Inc. is under review by the IRS. We expect the examination for this tax yearexaminations to be completed within the nextduring fiscal year 122022. months. 

 

Since we are subject to audit by various taxing authorities, it is reasonably possible that the amount of unrecognized tax benefits will change during the next 12 months. However, we do not expect the change, if any, to have a material effect on our financial condition or results of operations within the next 12 months.

 

Page 13

 

Note 1110. Commitments and Contingencies

 

We review the adequacy of our legal reserves on a quarterly basis and establish reserves for loss contingencies that are both probable and reasonably estimable. As of December 31, 2020September 30, 2021, there were no material legal reserves recorded on the accompanying unaudited Condensed Consolidated Balance Sheets. 

Under the terms of the revised IBP agreement, we are required to pay contingent consideration if the company is able to achieve certain operational and regulatory milestones. The potential undiscounted consideration payable ranges from €0 to €450, depending on whether units being developed are certified for sale by U.S. and foreign regulatory bodies. We currently believe that it is more likely than not that all aspects of the contingency will be achieved, and we expect to pay $555, depending on foreign exchange rates, during the year ending March 31, 2021.

 

Companies are required to collect and remit sales tax from certain customers if the company is determined to have nexus in a particular state. The determination of nexus varies by state and often requires technical knowledge of each jurisdiction's tax case law. During thefiscal year nine2021, months ended December 31, 2020, we determined that certain subsidiaries of GPT had established nexus in various jurisdictions during prior periods without properly collecting and remitting sales tax, and in certain cases had collected sales tax and not remitted it. We estimate the total net exposure including interest and penalties is $2,501, whichThe estimated accrued liability for this matter is included in other accrued expenses on the condensed consolidatedCondensed Consolidated Balance Sheets. The balance sheet.was $2,700 and $2,714 as of September 30, 2021 and March 31, 2021, respectively. The balance decreased because we settled our obligations with certain states during the six months ended September 30, 2021, partially offset by additional taxes, interest, and penalties incurred. Approximately $1,899 of the liability is considered a preacquisition contingency and iswas included in purchase accounting, which is described in further detail in Note 12. "Significant Transactions". The remainder of the liability represents $405 of sales tax payable for sales made in states where we have established nexus and $196 of interest incurred on the liabilities subsequent to the date of acquisition.accounting. 

 

 

Note 1211. Significant Transactions

 

GPT AcquisitionAgena Bioscience, Inc.

On October 31, 2019,20, 2021, we completed the acquisition of 100% of the outstanding shares of GPT, which comprises our new reportable segment - Biopharmaceutical Development. The acquisition of GPT expanded our presence intoAgena. Agena is a new market--immunoassaysleading clinical genomics tools company that develops, manufactures, and peptide synthesis solutions--that accelerate the discovery,supplies highly sensitive, low-cost, high-throughput, genetic analysis solutions to clinical labs and development and manufacturing of biotherapeutic drugs. GPT systems include laboratory instruments, consumables, kits, and software that maximize laboratory productivity by miniaturizing and automating immunoassays at nanoliter scale. GPT's protein detection is used most frequently by pharmaceutical and biotech companies that are developing protein-based drugs. This division also provides instruments, consumables, and software for the chemical synthesis of peptides from amino acidswhich are used in the discovery of new peptide-based drug therapies.  After adjustments, we paid cash consideration of $181,547 to the sellers in the transaction.  The acquisition was considered a stock purchase for tax purposes.partners globally. 

 

Fair Value of Net Assets Acquired

We accounted for the GPT Acquisition as the purchase of a business and GPT's results of operations have been included in our consolidated statements of operations and cash flows from the date of acquisition. Under the acquisition method of accounting, the net assets of GPT were initially recorded as ofOn the acquisition date, at their respective estimated fair values, using information obtained during due diligenceAgena shareholders were entitled to an aggregate cash purchase price of $300,000, subject to customary purchase price adjustments, and from other sources, and consolidated with those of Mesa Labs.  We refined our valuation models, assumptions, and inputs based on additional information obtained subsequentthat amount was remitted to the closing ofpaying agent or other third parties. We funded the transaction relatedusing cash on hand, combined with the proceeds from a $70,000 draw under our Credit Facility. Refer to factsNote 6. "Indebtedness" for additional details on our Credit Facility. The initial accounting for Agena is not complete due to the limited amount of time since the acquisition date. In an acquisition, U.S. GAAP requires the company to record all assets acquired and circumstances that existedall liabilities assumed at the acquisition date fair value. We are in order to estimate fair value more accurately for the purchase price allocation. The preparationprocess of the valuation required the use of Level 3 inputs, which are subject to significant assumptions and estimates. Critical estimates included, but were not limited to, future expected cash flows, including projected revenues and expenses, and the applicable discount rates. 

During the three months ended December 31, 2020, we finalized the valuation of net assets acquired. The significantpreparing our preliminary purchase price allocation, changes duringincluding initial estimates for inventory, goodwill, and intangible assets. 

Butler, New Jersey Closure

We completed the nine months ended December 31, 2020 included: a net decreasepreviously-announced closure of $6,002 in the value of intangible assets; a decrease of $3,752 in the value of the inventory step-up; an increase of $878 in the value of property, plant and equipment, net; and an increase of $1,899 to other accrued expenses and $500 to accounts receivable, net related to sales tax obligations of GPT that were partially indemnified in our sale and purchase agreement. See Note 11. "Commitments and Contingencies" for more information on the sales tax liability. We also made adjustments to deferred tax assets and deferred tax liabilities primarily due to the tax effect of these changes to the purchase price allocation. During the nine months ended December 31, 2020, the cumulative net decrease to amortization expense recorded as a result of the decrease to intangible assets was $344, of which $178 of expense was recorded to cost of revenues and a benefit of $522 was recorded in general and administrative costs. Additionally, a $207 cumulative increase to depreciation expense was recorded to general and administrative costsButler, New Jersey facility during the three months ended SeptemberJune 30, 20202021. asThe facility was primarily used in the production of our gas flow calibration and air sampling equipment, which is part of our Instruments division. Our manufacturing facility in Lakewood, Colorado is currently undergoing renovations that will allow it to accommodate the production of the gas flow calibration and air sampling equipment. Consolidating the production of these products is expected to reduce facilities costs and streamline our use of lean manufacturing tools under central management to further encourage production efficiencies.

As a result of the increasefacility consolidation, we incurred $77 of severance costs during the six months ended September 30,2021 which were recorded to cost of revenues, selling, and general and administrative expense on the Consolidated Statement of Income. As of September 30, 2021, a total of $70 remained outstanding and accrued, which relates to severance costs. We do not expect to incur any material expenses related to the Butler, New Jersey consolidation in the fair value of property, plant and equipment. future periods.

 

Page 14

The cumulative impacts of all adjustments have been reflected in the unaudited condensed consolidated financial statements as of and for the nine months ended December 31, 2020. The components and allocation of the purchase price consist of the following amounts:

 

 

Note

 

Fair Value

 

Cash and cash equivalents

  $4,654 

Accounts receivable

(a)

  6,663 

Inventories

(b)

  12,522 

Prepaid income taxes

   477 

Prepaid expenses and other

   14,149 

Property, plant and equipment

   1,523 
Other assets   1,469 
Deferred taxes   10,576 

Intangible assets:

     

Customer relationships

(c)

  77,500 

Trade name

(c)

  4,600 

Non-compete agreements

(c)

  0 

Acquired technology

(c)

  11,800 

Goodwill

(d)

  85,130 

Total Assets acquired

  $231,063 
      

Accounts payable

   599 

Accrued salaries and payroll taxes

   10,735 

Other short-term liabilities

   157 

Unearned revenues

   2,089 

Other accrued expenses

   6,967 

Deferred taxes

   23,350 
Other long-term liabilities   965 

Total liabilities assumed

  $44,862 
      

Total closing amount, net of cash acquired

  $181,547 

(a)

Accounts receivable is composed of trade accounts receivable, net which is expected to be collected. 

(b) 

Finished goods inventory of GPT includes $8,066 of inventory-step up, which is required to report inventory at fair value at the time of acquisition. The inventory step-up was amortized to cost of revenues over approximately eight months following the acquisition date, which resulted in a temporary reduction in gross profit for the business. During the period from November 1, 2019 until March 31, 2020, we recorded $8,502 of amortization of inventory step-up costs in cost of revenues on the Condensed Consolidated Statements of Operations. The final inventory valuation was completed during the nine months ended December 31, 2020 and was lower than our preliminary valuation, resulting in a cumulative effect decrease of $436 in amortization of inventory step up costs. 

(c)

Customer relationships and acquired technology are being amortized on a straight-line basis over a 10 year period. Amortization expense for customer relationships is recorded to general and administrative expenses; amortization expense for acquired technology is recorded to cost of revenues. During the nine months ended December 31, 2020, $5,328 of amortization expense related to the GPT intangible assets was recorded to general and administrative costs and $1,101 of amortization expense was recorded to cost of goods sold and allocated to the Biopharmaceutical Development division, including the cumulative-effect benefit to amortization expense discussed above. Trademarks associated with this acquisition are considered indefinite-lived intangibles. The estimated fair value of identifiable intangible assets was determined primarily using the income approach, which requires a forecast of all the expected future cash flows associated with the identified intangible assets. 

(d)

Acquired goodwill of $85,130, all of which is allocated to the Biopharmaceutical Development reportable segment, represents the value expected to arise from organic revenues growth projections that are expected to exceed that of our legacy divisions, and the opportunity to expand into a new market with well-established market share. The goodwill acquired is not deductible for income tax purposes.

Unaudited Pro Forma Information

GPT's operations contributed $23,863 to revenues and ($7,370) of net loss to our consolidated results during the nine months ended December 31, 2020 including cumulative-effect adjustments. The loss includes over $6,000 in amortization of intangibles acquired in a business combination and over $4,000 of realized and unrealized losses on foreign currency. We included the operating results of GPT in our Condensed Consolidated Statements of Operations beginning on November 1, 2019, subsequent to the acquisition date. The following pro forma financial information presents the combined results of operations of Mesa Labs and GPT as if the acquisition had occurred on April 1, 2019 after giving effect to certain pro forma adjustments. The pro forma adjustments reflected only include those adjustments that are directly attributable to the GPT Acquisition, factually supportable and have a recurring impact; they do not reflect any adjustments for anticipated expense savings resulting from the acquisition and are not necessarily indicative of the operating results that would have actually occurred had the transaction been consummated on April 1, 2019 or of future results. 

  

Three Months Ended December 31,

  

Nine Months Ended December 31,

 
  

2019

  

2019

 

Pro forma total revenues (1)

 $35,190  $103,097 

Pro forma net income (2)

  2,226   8,661 

(1) Net revenues were adjusted to include net revenues of GPT. 

(2) Pro forma adjustments to net earnings attributable to Mesa Labs include the following:

Excludes interest expense attributable to GPT's external debt that was paid off as part of the acquisition.

Additional depreciation expense of $66 based on the increased fair value of property, plant and equipment.

Additional amortization expense of $4,801 for the nine months ended December 31, 2019 based on the increased fair value of amortizable intangible assets acquired, net of adjustments.

For the nine months ended December 31, 2019, $358 additional stock based compensation expense representing expense for performance share units awarded to certain key GPT employees net of actual forfeitures.

Income tax effect of the adjustments made at a blended federal and state statutory rate (approximately 25%).

Page 15

 

Note 1312. Segment Information

 

As of December 31, 2020September 30, 2021, we had four4 reportable segments,segments: Sterilization and Disinfection Control, Instruments, Biopharmaceutical Development, Instruments, and Continuous Monitoring. Results for the Cold Chain Packaging division, which we exited during the year ended March 31, 2020, are now presented within Corporate and Other. The following tables set forth our segment information: 

 

  

Three Months Ended December 31, 2020

 
  

Sterilization and Disinfection Control

  

Instruments

  

Biopharmaceutical Development

  

Continuous Monitoring

  

Corporate and Other

  

Total

 

Revenues (1)

 $13,077  $8,971  $8,711  $3,413  $0  $34,172 

Gross profit (loss)

 $9,308  $5,368  $4,616  $1,501  $(140) $20,653 

Reconciling items (2)

                      (26,380)

(Loss) before income taxes

                     $(5,727)

  

Three Months Ended December 31, 2019

 
  

Sterilization and Disinfection Control

  

Instruments

  

Biopharmaceutical Development

  

Continuous Monitoring

  

Corporate and Other

  

Total

 

Revenues (1)

 $11,619  $10,014  $5,637  $4,156  $229  $31,655 

Gross profit (loss)

 $8,101  $6,526  $(1,294) $1,488  $(18) $14,803 

Reconciling items (2)

                      (19,880)

(Loss) before income taxes

                     $(5,077)

  

Nine Months Ended December 31, 2020

 
  

Sterilization and Disinfection Control

  

Instruments

  

Biopharmaceutical Development

  

Continuous Monitoring

  

Corporate and Other

  

Total

 

Revenues (1)

 $37,696  $24,209  $23,791  $10,277  $0  $95,973 

Gross profit (loss)

 $28,098  $14,909  $15,294  $4,053  $(76) $62,278 

Reconciling items (2)

                      (64,867)

(Loss) before income taxes

                     $(2,589)

 

Nine Months Ended December 31, 2019

  

Three Months Ended September 30,

  

Six Months Ended September 30,

 
 

Sterilization and Disinfection Control

  

Instruments

  

Biopharmaceutical Development

  

Continuous Monitoring

  

Corporate and Other

  

Total

  

2021

  

2020

  

2021

  

2020

 

Revenues (1)

 $35,823  $28,518  $5,637  $11,059  $2,442  $83,479 

Total revenues (a)

        

Sterilization and Disinfection Control

 $14,033  $11,552  $29,183  $24,619 

Biopharmaceutical Development

 10,555  9,131  19,432  15,080 

Instruments

 6,970  7,558  14,532  15,238 

Continuous Monitoring

  4,282   3,619   7,613   6,864 

Total revenues (a)

 $35,840  $31,860  $70,760  $61,801 
 
Gross profit (loss) $25,334 $18,164 $(1,294) $3,994 $395 $46,593         

Reconciling items (2)

             (42,471)

Sterilization and Disinfection Control

 $10,486  $8,770  $21,914  $18,790 

Biopharmaceutical Development

 6,601  6,212  11,293  10,678 

Instruments

 4,112  4,852  8,772  9,541 

Continuous Monitoring

  2,016   1,368   3,468   2,552 

Reportable segment gross profit

 23,215  21,202  45,447  41,561 

Corporate and Other (b)

  (75)  83   (96)  64 

Gross profit

 $23,140  $21,285  $45,351  $41,625 

Reconciling Items:

 

Operating expenses

  18,939   16,815   38,027   33,585 

Operating income

 4,201  4,470  7,324  8,040 

Nonoperating (income) expense, net

  (342)  2,086   1,363   4,902 

Earnings before income taxes

            $4,122  $4,543  $2,384  $5,961  $3,138 

 

 

(1)(a)

Intersegment revenues are not significant and are eliminated to arrive at consolidated totals.

 

(2)(b)

Reconciling items include selling, generalNon-reportable operating segments and administrative, researchunallocated corporate expenses are reported within Corporate and development, interest expense and amortization of debt discount, and other (income) expenses.

Other. 

 

The following table sets forth assetsinventories by reportable segment:segment. Our chief operating decision maker is not provided with any other segment asset information. 

 

  

December 31, 2020

  

March 31, 2020

 

Sterilization and Disinfection Control

 $71,706  $73,103 

Instruments

  29,967   31,025 

Biopharmaceutical Development

  205,769   182,758 

Continuous Monitoring

  28,834   29,732 

Corporate and administrative

  285,360   103,588 

Total

 $621,636  $420,206 

The increase in total assets was primarily attributable to $145,935 of cash proceeds resulting from the sale and issuance of 600,000 shares of our common stock during the nine months ended December 31, 2020, discussed in Note 8. "Stockholders' Equity", as well the effect of foreign currency translation on assets. 

  

September 30,

  

March 31,

 
  

2021

  

2021

 

Sterilization and Disinfection Control

 $2,187  $2,333 

Biopharmaceutical Development

  3,706   4,162 

Instruments

  4,566   3,253 

Continuous Monitoring

  1,658   1,430 

Total inventories

 $12,117  $11,178 

 

 

Note 1413. Subsequent EventsEvent

 

InAs disclosed in our Form January8-K filed on October 29, 2021, we announced that ourthe Compensation Committee of Mesa's Board of Directors declaredgranted a quarterly cash dividendspecial long-term equity award (the “Special Award”) to Gary Owens, Chief Executive Officer and Member of $0.16 per sharethe Board of commonDirectors on October 28, 2021. The Special Award consists of an award of performance stock payableunits covering a target of 40,000 shares (“PSUs”) that is subject to both performance and service conditions. The performance period of the award is the three-year period from April 1, 2021 through March 31, 2024 and the service period is the period commencing October 28, 2021 and ending on March 15, 2021,October 27, 2024, October 27, 2025, and October 27, 2026 on which dates eligible PSUs will vest and be distributed to shareholders of record at the close of business on February 26, 2021.Mr. Owens. 

 

 

Page 1615

 

Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations

(Dollars in thousands, except per share amounts)

 

Forward Looking Statements

 

ThisQuarterlyReport on Form 10-Qcontains forward-looking statements which are made pursuant to the safe harbor provisions of Section27A of the Securities Act of 1933, as amended, and Section21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”Exchange Act). The forward-looking statements in this Quarterly Report on Form 10-Qdo not constitute guarantees of future performance. Investors are cautioned that statements in this Quarterly Report on Form 10-Qwhich are not strictly historical statements, including, without limitation, express or implied statements or guidance regarding current or future financial performance and position, potential impairment of future earnings, anticipated effects of, and future actions to be taken in response to, the COVID-19 pandemic, management’spandemic; results of acquisitions; managements strategy, plans and objectives for future operations or acquisitions, product development and sales,sales; product candidate research development and development; regulatory approval,approval; selling, general and administrative expenditures,expenditures; intellectual property,property; development and manufacturing plans,plans; availability of materials and productcomponents; and adequacy of capital resources and financing plans constitute forward-looking statements. These forward-looking statements are based on current expectations, estimates, forecasts and projections about the industry and markets in which the Company operates, and management’smanagements beliefs and assumptions. The Company undertakes no obligation to publicly update or revise the statements in light of future developments. In addition, other written and oral statements that constitute forward-looking statements may be made by the Company or on the Company’sCompanys behalf. Words such as “expect,expect,intend,” “seek,seek,plan,” “anticipate,anticipate, “intend,believe, “plan,could, “believe,estimate, “could,may, “estimate,target, “may,project, “target,” “project,” or variations of such words and similar expressions are intended to identify forward-looking statements. Such forward-looking statements are subject to a number of risks and uncertainties that could cause actual results to differ materially from those anticipated, including risks associated with: the duration and impact of the COVID-19 pandemic and the myriad of its adverse effects on our business including related decreases in customer demand and spending;business; our ability to successfully grow our business, including as a result of acquisitions; the results on operations of acquisitions; our ability to consummate acquisitions at our historical rate and at appropriate prices, and our ability to effectively integrate acquired businesses and achieve desired results; the market acceptance of our products; technological or market viability of our products; reduced demand for our products that adversely impacts our future revenues, cash flows, results of operations and financial condition; inability to consummate acquisitions at our historical rate and at appropriate prices, and to effectively integrate acquired businesses;products; conditions in the global economy and the particular markets we serve; significant developments or uncertainties stemming from the U.S. government,governments, including changes in U.S. trade policies and medical device regulations; the timely development and commercialization, and customer acceptance, of enhanced and new products and services; retirement of old products and customer migration to new products; projections of revenues, growth, operating results, profit margins, expenses, earnings, margins, tax rates, tax provisions, cash flows, liquidity, demand, and competition; the effects of additional actions taken to become more efficient or lower costs; restructuring activities;laws regulating fraud and abuse in the health care industry and the privacy and security of health and personal information; product liability; information security; outstanding claims, legal proceedings,and regulatory proceedings; international business challenges and regulations including anti-corruption and sanctions laws; tax audits and assessments and other contingent liabilities; and foreign currency exchange rates and fluctuations in those rates.  Further information on potential riskrates; general economic, industry, and capital markets conditions; the timing of any of the foregoing; assumptions underlying any of the foregoing; and any other statements that address events or developments that we intend or believe will or may occur in the future.Such risks and uncertainties also include those listed in Item 1A. Risk Factors, and elsewhere in this report.The foregoing list sets forth many, but not all, of the factors that could affectimpact our financialability to achieve results are includeddescribed in the filings made by us from time to time with the Securities and Exchange Commission including under the section entitled “Risk Factors” in our Annual Report on Form 10-K, for the year ended March 31, 2020 and our subsequent Quarterly Reports on Form 10-Qs. any forward-looking statements.We undertake nodisclaim any obligation to publicly update any forward-looking statement, whether as a result of new information, future developments or otherwise, except as may be required by law.otherwise.

 

Business Overview

 

We are a multinational manufacturer, developer, and seller of life science tools and critical quality control products and services, many of which are sold into niche markets that are driven by regulatory requirements. We have manufacturing operations in North Americathe United States and Europe, and our products are marketed by our sales personnel in North America, Europe, China, Japan,and Asia, and by independent distributors in these areas as well as throughout the rest of the world. We prefer markets in which we can establish a strong presence and achieve high gross margins. As of December 31, 2020,September 30, 2021, we managed our operations in four reportable segments, or divisions: Sterilization and Disinfection Control, Instruments, Biopharmaceutical Development, Instruments, and Continuous Monitoring, each of which are described further in Results"Results of OperationsOperations" below. Non-reportable operating segments (including our Cold Chain Packaging division which ceased operations during the year ended March 31, 2020) and unallocated corporate expenses are reported within Corporate and Other.

As discussed in Note 8. "Stockholders' Equity" within Item 1. "Financial Statements," we completed an equity offering of our common stock, which provided $145,935, net of discounts and issuance costs. We intend to use the money raised for general corporate purposes, which may include furthering our acquisition strategy.

 

Corporate Strategy

We strive to create shareholder value and further our purpose of Protecting the Vulnerable® by growing our business both organically and through further acquisitions, by improving our operating efficiency, and by continuing to hire, develop and retain top talent. As a business, we commit to our purpose of Protecting the Vulnerable® every day by taking a customer-focused approach to developing, building, and delivering our products. We serve a broad set of industries, in particular the pharmaceutical, healthcare, and medical device industries, that require dependable quality control and calibration solutions to ensure the safety and efficacy of the products they use, and by delivering the highest quality products possible, we are committed to protecting people, the environment, and end products.

 

Our revenues come from product sales, which includes hardware, software, and consumables; as well as services, which include installation, discrete maintenance services, and ongoing maintenance contracts.Organic Revenues increase as a result of organic or inorganic revenues growth. InorganicGrowth

Organic revenues growth is primarily driven by acquisitions.the expansion of our customer base, increases in sales volumes, and price increases. Our ability to increase organic revenues is affected by general economic conditions, both domestic and international, customer capital spending trends, competition, and the introduction of new products. We typically evaluate costs and pricing annually. Our policy is to price our products competitively and, where possible, we pass along cost increases to our customers in order to maintain our margins.

Page 16

Inorganic Revenues Growth - Acquisitions

Over the past decade, we have consummated a number of acquisitions as part of our growth strategy. The acquisitions of these businesses, which are in addition to organic revenues growth, have allowed us to expand our product offerings, globalize our company, and increase the scale at which we operate, which in turn affords us the ability to improve our operating efficiency, extend our customer base, and further the pursuit of our purpose: Protecting the Vulnerable®. On October 20, 2021, we announced the completion of the acquisition of Agena for an aggregate purchase price of $300 million, subject to customary purchase price adjustments. Agena is a leading clinical genomics tools company that develops, manufactures, and supplies highly sensitive, low-cost, high-throughput, genetic analysis solutions to clinical labs and development partners globally. The acquisition of Agena accelerates Mesa's strategic trajectory towards higher growth applications within the regulated segments of the life sciences tools market. Going forward, we expect the substantial majority of our revenues to be generated from sales to pharmaceutical, healthcare service, and medical device verticals. 

 

Improving Our Operating Efficiency

We continue to focus on improvingmaximize value in both our operating efficiencyexisting businesses and those we acquire by implementing efficiencies in our manufacturing, commercial, engineering, and administrative operations. We achieve efficiencies using the four pillars that make up The Mesa Way, which is our customer-centric, lean basedlean-based system for continuously improving and operating a set of high-margin, niche businesses. The Mesa Way is based on four pillars:focused on: Measuring What Matters using our customers' perspective and setting high standards for performance; Empowering Teams to improve operationally and exceed customer expectations; Steadily Improving using lean-based tools designed to help us identify the root cause of opportunities and prioritize the biggest opportunities; and Always Learning so that performance continuously improves. 

 

Measure what matters: We use “True North,” our customer’s perspective, to measure what matters most to customers and to set high standards for performance. We manage to leading indicators, whenever possible, which drives us to proactively avoid problems before they

Hire, Develop, and Retain Top Talent

At the center of our organization are talented people who are apparent to our customers.

Empower Teams: We move decision making as close to the customer as possible and provide the structure and real-time communication forum to align the whole organization towards surpassing customer expectations.

Steadily Improve: We leverage a common and proven set of lean-based tools to identify the root cause of opportunities, prioritize our biggest opportunities, and enable change to be embraced and implemented quickly.

Always Learn:  We ensure that improvements are sustained, enabling us to raise performance expectations and repeat the cycle of improvement. Equally, this cycle strengthens the Mesa team by providing endless learning opportunities for our employees and helps us to become an employer of choice in our communities.

Finally, we hire, develop, and retain top talent, capable of taking on new challenges using a team approachapproach. It is our exceptionally talented workforce that works together and uses our lean-based tool set to find ways to continuously improve our products, our services, and ourselves, resulting in long-term value creation for our shareholders. 

 

Page 17

COVID-19Business Update and Business UpdateCOVID-19

During March 2020, the impact from the spreadingspread of COVID-19 was declared a global pandemic by the World Health Organization and a national public health emergency in the United States. The consequencesWe continue to monitor the pandemic, including the current spread of certain variants of the outbreakvirus, and we have taken and will continue to take steps to identify and mitigate the adverse impact on, and risks to, our business (including but not limited to our employees, customers, vendors, manufacturing capabilities and capacity, and supply and distribution channels) posed by the economyspread of COVID-19 and the government responses thereto.

The COVID-19 pandemic began to impact our business late in fiscal year 2020, and its impacts affected our business in various ways throughout fiscal year 2021 and to some extent, into the first two quarters of fiscal year 2022. The pandemic and related public health recommendations and mandated precautions to mitigate the spread of COVID-19, including regulations to close or limit the operating hours of our laboratory and other customers, and to prevent non-essential personnel from going on-site to customer locations to service or market our products, have continued to evolve throughoutnegatively affected our operations. Specifically, during fiscal year 2021 the nineBiopharmaceutical Development division, the Instruments division, and the Continuous Monitoring division were materially negatively impacted. While many recommendations and precautions that affected us in fiscal year 2021 have been rescinded in the United States, some regulations impacting our operations, particularly in Europe, affected our operations during the six months ended December 31, 2020September 30, 2021, and continue to do so. Additionally, we are unable to ascertain the full extent of the impact on our business as of the date of this filing. Throughout our fiscal year, the pandemic has continued to present substantial public health and economic challenges around the world and is affecting our employees, business operations, and operating segments in various ways.

As COVID-19 has continued to spread and significantly affect markets around the world, we have continued to enforce company policiesbelieve that are focused on ensuring the safetymacroeconomic uncertainties that caused some of our employees while also delivering our goodscustomers to customers acrossdefer the world. Due to the critical naturepurchase of our products and services, we are generally exempt from governmentalpersisted into the first quarter of fiscal year 2022, primarily affecting our Instruments division although, orders in the U.S. and other countries requiring businessesdivision have increased during fiscal year 2022 to suspend operations. Nevertheless, the pandemic brought a material disruption to our operations. To protect employees and comply with regulations and recommendations to limit gatherings and increase social distancing, we require office-based employees to work remotely in most cases, and we implemented enhanced safety protocols at our manufacturing facilities, including performing health checks at the start of shifts, utilizing contact tracing technology to support case investigation when needed, and maximizing the amount of space between workspaces. We have taken aggressive steps to limit the exposure and enhance the safety of our facilities for employees working so that we can continue to supply products and services to our customers, although there is no guarantee that our measures will be successful. Additionally, we continue to evaluate and monitor the condition of our supply chain and work with our suppliers to develop contingency plans for potential supply interruptions. date.

Our business has encountered challenges resulting from COVID-19, as the global downturn resulted in a slow-down in demand for many of the products and services that we offer. The impact on our businesses is outlined below:

Sterilization and Disinfection Control: This division's revenues have been inconsistent during the nine months ended December 31, 2020, which we believe is attributable to customers' reactions to COVID-19. The division benefited in the three months ended June 30, 2020 from fulfilling temporary advanced buying orders placed by certain customers during the three months ended March 31, 2020; however, overall orders slowed significantly during the latter part of the three months ended June 30, 2020 and continued to slow throughout the three months ended September 30, 2020 as advanced ordering began to reverse and customers used stock that they had purchased previously. During the three months ended December 31, 2020, revenues began to increase again as many customers depleted their stock and resumed ordering at more normal levels. We believe that the consumable, critical, and disposable nature of Sterilization and Disinfection Control products renders them less sensitive to general economic conditions, and the demand for Sterilization and Disinfection Control products has remained relatively strong. Prior to the COVID-19 pandemic, the worldwide market for sterilization and disinfection control products had been growing as countries increase focus on verifying the effectiveness of sterilization and disinfection processes.

Biopharmaceutical Development: Demand for hardware, consumables, and services sold by our Biopharmaceutical Development division declined during the start of the pandemic (the three months ended June 30, 2020), which we believe was mainly a result of COVID-19. Subsequently, as several of the restrictions limiting vendors from being on-site at customer facilities were eased during the summer and fall of 2020, demand for Biopharmaceutical Development products and services increased significantly compared to the three months ended June 30, 2020, but the global pandemic continues to inhibit our ability to use proven strategies to market and sell these products.  Further, increases in COVID-19 cases throughout the world have caused customers, including laboratories to reduce capacity or close completely, resulting in decreased demand for our products. In the future, when travel and gathering restrictions are lifted and we are permitted on-site at more customer facilities, and when laboratories globally are open for normal operations, we expect an opportunity for greater organic revenue growth in the Biopharmaceutical Development division.

Continuous Monitoring: Demand for hardware and software sold by our Continuous Monitoring division declined during the start of the pandemic (the three months ended June 30, 2020), which we believe was mainly a result of COVID-19. As restrictions limiting vendors from being on-site at customer facilities were eased during our second fiscal quarter, demand for Continuous Monitoring products and services increased somewhat compared to the three months ended June 30, 2020, some of which was a result of fulfilling backlog we were restricted from completing during the three months ended June 30, 2020.  Although orders have increased steadily as our fiscal year has progressed, the global pandemic continues to inhibit our ability to install these products. Further, increases in COVID-19 cases throughout the U.S. and Canada could lead to customers further tightening facility access, resulting in decreased demand for our products. In the future, when travel and gathering restrictions are lifted more broadly and we are able to go on-site at more customer facilities, we expect to continue to grow revenues organically in the Continuous Monitoring division.

Instruments: Demand for hardware and certain services sold by our Instruments division declined during the nine months ended December 31, 2020 as compared to the nine months ended December 31, 2019, which we believe was mainly a result of COVID-19 due to the discretionary nature of many instruments purchases. However, beginning late in September, 2020, and continuing through the three months ended December 31, 2020, we began to see demand for these products increase somewhat, and revenues increased as we fulfilled orders. Although demand for hardware sold by our Instruments division appears to be beginning to improve as customers resume making discretionary capital purchases, we continue to expect that it will be several quarters before demand and revenues recover.  

 

Sales of our hardware products have historically been more sensitive to general economic conditions than sales of our consumables. The COVID-19 induced economic downturn appears to be having a similar impact, as businesses are postponing certain capital spending in response to economic uncertainty, declines in income and asset values, tighter credit, unemployment, and negative financial news. Even as the broad healthcare industry has begun to return to more normal operations resulting in increased sales levels in some of our divisions, outbreaks and increasing numbers of COVID-19 cases in many areas especiallyof the U.S. and Europe,world have and may continue to result in the reinstatement of strict regulations, which we expect would result in lower sales levels. We believe that COVID-19 related uncertainties, restrictions, and suppressed demand willmay continue to negatively impact our business during the remainder of thefiscal year ending March 31, 2021, and continuing into our year ending March 31, 2022. Even after the COVID-19 pandemic has subsided as a public health matter, we may experience material adverse impacts to our business as a result of its adverse impact on the global economy, in-person collaboration and sales efforts, and our customers’ changed purchasing behavior and confidence.

 

GrossCOVID-19 has also caused broad market phenomena such as supply chain disruptions, inflation, and wage pressure to which we are susceptible. Currently, supply chain constraints are affecting the ability of suppliers to provide components used to manufacture certain of our products.  We experienced increased supply constraints for certain components used in our operations, particularly components used by the Instruments division. We continue to work with our suppliers to understand the existing and potential future impacts to our supply chain and are taking actions in an effort to mitigate such impacts, including pre-ordering components in higher quantities than usual, which has resulted in increased raw materials balances on our balance sheet as of September 30, 2021. However, during the quarter ended September 30, 2021, we were more impacted by our inability to acquire various components on a timely basis, which is discussed in more detail in our "Results of Operations" and "Risk Factors" below. We expect disruptions to our supply chain to persist for at least the next four to six fiscal quarters. 

Apart from COVID-19, gross profit is affected by many factors including our product mix, manufacturing efficiencies, foreign currency rates, and price competition. Historically, as we have integrated our acquisitions and taken advantage of manufacturing efficiencies, our gross profit percentages for some products have improved. There are, however, differences in gross profit percentages between product lines, and ultimately the mix of sales will continue to impact our overall gross profit.

 

We completed the previously-announced closure of our Butler, New Jersey facility during the quarter ended June 30, 2021. The facility was primarily used in the production of our gas flow calibration and air sampling equipment, which is part of our Instruments division. We are continuing the integration process into our Lakewood, Colorado manufacturing facility. In addition, our Lakewood facility is currently undergoing renovations that will allow it to better accommodate the production of the gas flow calibration and air sampling equipment. Consolidating the production of these products is expected to reduce facilities costs and streamline our use of lean manufacturing tools under central management to further encourage production efficiencies.

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Results of Operations

 

Our results of operations and period-over-period changes are discussed in the following section. The tables and discussion below should be read in conjunction with the accompanying Unaudited Condensed Consolidated Financial Statements and the notes thereto appearing in Item 1. Financial Statements (in thousands, except percent data).

 

Revenues from our reportable segments increased 9%12% and 18%, organic14% for the three and six months ended September 30, 2021, respectively. The revenues growth was 1% and declined 3%, and grossentirely a result of organic revenues growth. Gross profit as a percentage of revenues increased 14decreased two percentage points and eightthree percentage points for the three and ninesix months ended December 31, 2020, asSeptember 30, 2021, respectively, compared to the three and ninesix months ended December 31, 2019,September 30, 2020, respectively. Results by reportable segment are as follows:

 

 

Revenues

  

Organic Revenues Growth

  

Gross Profit as a % of Revenues

  

Revenues

  

Organic Revenues Growth

  

Gross Profit as a % of Revenues

 
 

Three Months Ended December 31, 2020

  

Three Months Ended December 31, 2019

  

Three Months Ended December 31, 2020

  

Three Months Ended December 31, 2019

  

Three Months Ended December 31, 2020

  

Three Months Ended December 31, 2019

  

Three Months Ended September 30, 2021

  

Three Months Ended September 30, 2020

  

Three Months Ended September 30, 2021

  

Three Months Ended September 30, 2020

  

Three Months Ended September 30, 2021

  

Three Months Ended September 30, 2020

 

Sterilization and Disinfection Control

 $13,077  $11,619  13% 1% 71% 70% $14,033  $11,552  21% (4%) 75% 76%

Biopharmaceutical Development

 10,555  9,131  16% N/A  63% 68%

Instruments

 8,971  10,014  (10%) 2% 60% 65% 6,970  7,558  (8%) (16%) 59% 64%

Biopharmaceutical Development

 8,711  5,637  14% N/A  53% (23%)

Continuous Monitoring

  3,413   4,156  (18%) 6% 44% 36%  4,282   3,619  18% 1% 47% 38%

Mesa Labs' reportable segments

 $34,172  $31,426  1% 2% 61% 47% $35,840  $31,860  12% (8%) 65% 67%

Corporate and Other

  -   229             

Total Company

 $34,172  $31,655                 

 

 

Revenues

  

Organic Revenues Growth

  

Gross Profit as a % of Revenues

  

Revenues

  

Organic Revenues Growth

  

Gross Profit as a % of Revenues

 
 

Nine Months Ended December 31, 2020

  

Nine Months Ended December 31, 2019

  

Nine Months Ended December 31, 2020

  

Nine Months Ended December 31, 2019

  

Nine Months Ended December 31, 2020

  

Nine Months Ended December 31, 2019

  

Six Months Ended September 30, 2021

  

Six Months Ended September 30, 2020

  

Six Months Ended September 30, 2021

  

Six Months Ended September 30, 2020

  

Six Months Ended September 30, 2021

  

Six Months Ended September 30, 2020

 

Sterilization and Disinfection Control

 $37,696  $35,823  5% 4% 75% 71% $29,183  $24,619  19% 2% 75% 76%

Biopharmaceutical Development

 19,432  15,080  29% N/A  58% 71%

Instruments

 24,209  28,518  (15%) 1% 62% 64% 14,532  15,238  (5%) (18%) 60% 63%

Biopharmaceutical Development

 23,791  5,637  14% N/A  64% (23%)

Continuous Monitoring

 10,277  11,059  (7%) 3% 39% 36%  7,613   6,864   11%  (1%)  46%  37%

Mesa Labs' reportable segments

 $95,973  $81,037  (3%) 3% 65% 57% $70,760  $61,801   14%  (6%)  64%  67%

Corporate and Other

  -   2,442             

Total Company

 $95,973  $83,479             

 

Our unaudited condensed consolidated results of operations are as follows:

 

 

Three Months Ended December 31,

  

Percentage

  

Nine Months Ended December 31,

  

Percentage

  

Three Months Ended September 30,

  

Percentage

  

Six Months Ended September 30,

  

Percentage

 
 2020 2019 Change 2020 2019 Change  

2021

  

2020

  

Change

  

2021

  

2020

  

Change

 

Revenues

 $34,172  $31,655  8% $95,973  $83,479  15% $35,840  $31,860  12% $70,760  $61,801  14%

Gross profit

 20,653  14,803  40% 62,278  46,593  34% 23,140  21,285  9% 45,351  41,625  9%

Operating expenses

  20,631   18,058  14%  54,216   39,697  37%  18,939   16,815   13%  38,027   33,585   13%

Operating income (loss)

 22  (3,255) (101%) 8,062  6,896  17%

Net (loss) income

 $(4,542) $(4,504)  1% $(646) $3,330   (119%)

Operating income

 4,201  4,470  (6%) 7,324  8,040  (9%)

Net income

 $3,720  $2,679   39% $5,715  $3,896   47%

 

Reportable Segments

 

Sterilization and Disinfection Control

Our Sterilization and Disinfection Control division manufactures and sells biological, cleaning, and chemical indicators. Biological, cleaning, and chemical indicators are used to assess the effectiveness of sterilization and disinfection processes in the hospital, dental, medical device, and pharmaceutical industries. The division also provides testing and laboratory services, mainly to the dental industry. Sterilization and disinfection control products are disposable and are used on a routine basis.

 

 

Three Months Ended December 31,

  

Percentage

  

Nine Months Ended December 31,

  

Percentage

  

Three Months Ended September 30,

  

Percentage

  

Six Months Ended September 30,

  

Percentage

 
 2020 2019 Change 2020 2019 Change  

2021

  

2020

  

Change

  

2021

  

2020

  

Change

 

Revenues

 $13,077  $11,619  13% $37,696  $35,823  5% $14,033  $11,552  21% $29,183  $24,619  19%

Gross profit

 9,308  8,101  15% 28,098  25,334  11% 10,486  8,770  20% 21,914  18,790  17%

Gross profit as a % of revenues

 71% 70% 1% 75% 71% 4% 75% 76% (1%) 75% 76% (1%)

 

Page 1918


 

Sterilization and Disinfection Control revenues increased 13%21% and 19% for the three and six months ended December 31, 2020 as manySeptember 30, 2021, respectively, which was achieved through effective efforts by our sales team to market and sell certain products to a larger customer base, particularly in Europe, volume increases with existing customers, and recovery of our customers resumed ordering at more normal levels. Revenues during the three months ended December 31, 2019 were lower than usual ashealthcare services markets, partially offset by a resultmodest strengthening of a supply disruption, creating a favorable comparison during the current year.  

Sterilization and Disinfection Control revenues increased 5% forU.S. dollar against the nine months ended December 31, 2020 as a result of organic revenues growth resulting from the timing of several large orders and modest price increases. euro.

 

Sterilization and Disinfection Control gross profit percentage increaseddecreased one percentage point and four percentage points for both the three and ninesix months ended December 31, 2020, respectively,September 30, 2021, primarily as a result of operating efficiencies from increased volumeproduct mix and favorable product mix.slightly higher production costs. 

 

Instruments

Our Instruments division designs, manufactures, and markets quality control instruments and consumable products utilized in the healthcare, pharmaceutical, food and beverage, medical device, industrial hygiene, and environmental air sampling industries. Instrument products have a longer life, and their purchase by our customers is discretionary, so sales are more sensitive to general economic conditions. Service demand is driven by our customers’ quality control and regulatory environments, which require periodic repair and recalibration or certification of our instrument products.

  

Three Months Ended December 31,

  

Percentage

  

Nine Months Ended December 31,

  

Percentage

 
  2020  2019  Change  2020  2019  Change 

Revenues

 $8,971  $10,014   (10%) $24,209  $28,518   (15%)

Gross profit

  5,368   6,526   (18%)  14,909   18,164   (18%)

Gross profit as a % of revenues

  60%  65%  (5%)  62%  64%  (2%)

Instruments revenues decreased 10% and 15% for the three and nine months ended December 31, 2020, respectively, as customers across all served markets continued to limit spending that is more discretionary in nature in response to economic uncertainty. However, we expect that the higher demand we experienced for our products during the three months ended December 31, 2020 does indicate that demand is beginning a slow return to more normal levels. 

Instruments gross profit percentage decreased five and two percentage points during the three and nine months ended December 31, 2020, respectively. The decrease resulted from a $212 charge for severance related to employees who work in our Butler, New Jersey facility which we intend to close during the three months ending June 30, 2021, lower revenues on a partially fixed cost base, and to a lesser extent, unfavorable product mix. 

Biopharmaceutical Development

Our Biopharmaceutical Development division was created as a result of the GPT acquisition on October 31, 2019. The division develops, manufactures, and sells automated systems for protein analysis (immunoassays) and peptide synthesis solutions. Immunoassays and peptide synthesis solutions accelerate the discovery, development, and manufacturing of biotherapeutic drugs. 

 

  

Three Months Ended December 31,

  

Percentage

  

Nine Months Ended December 31,

  

Percentage

 
  2020  2019  Change  2020  2019  Change 

Revenues

 $8,711  $5,637   55% $23,791  $5,637   322%

Gross profit (loss)

  4,616   (1,294)  457%  15,294   (1,294)  1282%
Gross profit (loss) as a % of revenues  53%  (23%)  76%  64%  (23%)  87%
  

Three Months Ended September 30,

  

Percentage

  

Six Months Ended September 30,

  

Percentage

 
  

2021

  

2020

  

Change

  

2021

  

2020

  

Change

 

Revenues

 $10,555  $9,131   16% $19,432  $15,080   29%

Gross profit

  6,601   6,212   6%  11,293   10,678   6%

Gross profit as a % of revenues

  63%  68%  (5%)  58%  71%  (13%)

 

The results of the Biopharmaceutical development division were consolidated into our results beginning on November 1, 2019. Although we did experience positive organic growth duringDevelopment's revenues increased 16% and 29% for the three and ninesix months ended December 31, 2020, Biopharmaceutical Development'sSeptember 30, 2021, respectively, due primarily increased sales of consumables as our laboratory customers were open for more normal operating hours in the first two quarters of fiscal year 2022 compared to the first two quarters of fiscal year 2021. The division's laboratory customers used significantly more consumables, driving 61% and 70% increases in consumables revenues were negatively impacted duringfor the three and ninesix months ended December 31, 2020 by economic uncertainty and social restrictions related to the COVID-19 pandemic.  Particularly during the three months ended JuneSeptember 30, 2020, and to2021, respectively. To a lesser extent, during the period from July 1, 2020 until December 31, 2020, global efforts to stop the spread of COVID-19 and the resulting shut down and slowing of many facets of our society and commerce resulted in reduced demand as we became unable to market our products at industry conferences or visit customers at their facilities. Additionally, many global laboratories that use this division's products continue to be closed or have limited hours. Restrictions limiting vendors from going on-site at customers facilities eased during the summer and fall of 2020. Additionally, during this time we increased efforts to pursue digital marketing avenues to continue to create leads and demonstrate our products to potential customers. As a result of loosening restrictions and our digital marketingsales efforts increased revenues duringin the second and third quarters of our fiscal year were significantly improved compared to our first quarter of our fiscal year.Biopharmaceutical Development division. 

 

Biopharmaceutical Development's gross profit percentage was 53%63% for the threequarter ended September 30, 2021. The gross profit percentage decreased as compared to the quarter ended September 30, 2020 as a result of a slightly unfavorable change in foreign exchange rates and higher labor costs, as well as unfavorable product mix. Biopharmaceutical Development's gross profit percentage was 58% for the six months ended December 31, 2020. September 30, 2021 as a result of a significantly unfavorable change in foreign exchange rates, the benefit of a positive $258 purchase accounting adjustment in the six months ended September 30, 2020, higher labor-related costs, and unfavorable product mix.

Substantially all of this division's sales are invoiced in either euros or U.S. dollars ("USD"); however, the majority of the costs in this division are recorded in Swedish Krona and translated to USD for reporting purposes. SinceThe USD was significantly weaker against the SEK during the quarter ended June 30, 2021 compared to the quarter ended June 30, 2020, and although the USD has weakened significantly against the Swedish Kronastrengthened to some extent during the three monthsquarter ended December 31, 2020,September 30, 2021, our reported costs in USD have increased substantially, while revenues have not benefited significantly from the change in currency valuation. Additionally,

Instruments

Our Instruments division designs, manufactures, and markets quality control instruments and consumable products utilized in the healthcare, pharmaceutical, food and beverage, medical device, industrial hygiene, and environmental air sampling industries. Instrument products have a longer life, and their purchase by our customers is discretionary, so sales are more sensitive to general economic conditions. Service demand is driven by our customers’ quality control and regulatory environments, which require periodic repair and recalibration or certification of our instrument products.

  

Three Months Ended September 30,

  

Percentage

  

Six Months Ended September 30,

  

Percentage

 
  

2021

  

2020

  

Change

  

2021

  

2020

  

Change

 

Revenues

 $6,970  $7,558   (8%) $14,532  $15,238   (5%)

Gross profit

  4,112   4,852   (15%)  8,772   9,541   (8%)

Gross profit as a % of revenues

  59%  64%  (5%)  60%  63%  (3%)

Instruments division revenues decreased 8% and 5% for the three and six months ended September 30, 2021, respectively, primarily as a result of supply and labor constraints, despite increased orders within the division. Particularly during the quarter ended September 30, 2021, we experienced constraints in the supply chain for components used in Instruments division products. Although fulfillment of some orders is delayed, to-date we have been able to retain the significant majority of our customers and orders. Separately, during the quarter ended June 30, 2021, order fulfillment of gas flow calibration and air sampling equipment was lower than the quarter ended June 30, 2020 as we worked to relocate the manufacturing of those items from our Butler, New Jersey facility to our Lakewood, Colorado facility, including hiring manufacturing employees to fulfill orders. 

Instruments gross profit percentage decreased five percentage points and three percentage points during the three and six months ended December 31, 2020, we revised our estimate of inventory overhead rates for this division, whichSeptember 30, 2021, respectively. The decrease in gross profit percentage resulted infrom lower revenues on a partially fixed cost base, higher periodlabor costs as lessa result of our overheada strong competition for employees in the labor market, increased costs were capitalized into inventory,for components and we wrote off inventory that we determined was obsolete. We expectsupplies, and to sell the remainder of the inventory produceda lesser extent, increased freight on purchased components. Supply chain disruptions are expected to continue for at the previously estimated rates overleast the next twofour to three quarters. Without thesix quarters, although these increased costs will negatively impact of the USD weakening and the inventory adjustmentsgross profit percentage only until we implement price increases to our customers during the three months ended December 31, 2020, we estimate that gross profit would have been 61%. Finally, unfavorable product mix negatively impacted gross profit margin percentage for this division during the three months ended December 31, 2020. fourth quarter of fiscal year 2022.

 

Page 2019


Biopharmaceutical Development's gross profit for the nine months ended December 31, 2020 includes a $436 reduction in amortization expense as a result of an adjustment booked to the value of an inventory step-up recorded in purchase accounting related to the GPT Acquisition. Gross profit for the nine months ended December 31, 2020 also includes $178 of incremental amortization expense related to the adjustment of the value of technology intangibles that are amortized to cost of revenues. Excluding the net impact of the amortization catch ups and the weakening of the USD, gross profit percentage would have been 65% for the nine months ended December 31, 2020. 

Biopharmaceutical Development gross profit (loss) margin was ($1,294) for the period from November 1, 2019 until December 31, 2019. The gross profit (loss) included $5,134 of amortization on an inventory step-up recorded in purchase accounting related to the GPT Acquisition. Excluding the step-up amortization, gross profit for the period ended December 31, 2019 would have been $3,840, and gross profit percentage would have been approximately 68%. 

 

Continuous Monitoring

Our Continuous Monitoring division designs, develops, and markets systems which are used to monitor various environmental parameters such as temperature, humidity, and differential pressure to ensure that critical storage and processing conditions are maintained in hospitals, pharmaceutical and medical device manufacturers, blood banks, pharmacies, and laboratory environments. Continuous monitoringMonitoring products and systems have a longer life, and their purchase by our customers is discretionary, so sales are sensitive to general economic conditions. Continuous monitoring products may be sold in conjunction with a perpetual or subscription-based software license, which may be required for the related hardware to function. Service demand is driven by our customers’ quality control and regulatory environments, which require periodic repair and recalibration or certification of our continuous monitoring systems.

 

 

Three Months Ended December 31,

  

Percentage

  

Nine Months Ended December 31,

  

Percentage

  

Three Months Ended September 30,

  

Percentage

  

Six Months Ended September 30,

  

Percentage

 
 2020 2019 Change 2020 2019 Change  

2021

  

2020

  

Change

  

2021

  

2020

  

Change

 

Revenues

 $3,413  $4,156  (18%) $10,277  $11,059  (7%) $4,282  $3,619  18% $7,613  $6,864  11%

Gross profit

 1,501  1,488  1% 4,053  3,994  1% 2,016 1,368 47% 3,468 2,552 36%

Gross profit as a % of revenues

 44% 36% 8% 39% 36% 3% 47% 38% 9% 46% 37% 9%

 

The Continuous Monitoring division's revenues decreasedincreased 18% and 11% for the three and six months ended December 31, 2020,September 30, 2021, due primarily to an increase in customers allowing access to their facilities as we completed several large orders during the three months ended December 31, 2019, resulting in a higher than usual revenues in the comparable period. Continuous Monitoring's revenues decreased 7% for the nine months ended December 31, 2020 as a result of the shut downour service technicians were able to go to client sites to complete service requests and slowing of many facets of the U.S. society and economy in response to the COVID-19 outbreak. Specifically, ourhardware installations. Our ability to go on-site to many of our customers facilities to install and service systems was severely restricted during April and May, 2020.  Overall, restrictions began to ease lateparts of the first six months of fiscal year 2021. As this division's sales are exclusively in our first fiscal quarter, which allowed our technicians to go on-site to perform work that was previously backlogged as a resultNorth America, the majority of COVID-19 related restrictions and our sales volumes began to increase during our second and third fiscal quarters; however, customer reaction to the acceleration of COVID-19 infections during our third fiscal quarter did negatively impactthat affected our ability to service customers and complete certain system installations. Overall, we continue to see strong demand, including market expansion as hospitals increase monitoring systemsgenerate revenue in response tofiscal year 2021 were relaxed during the COVID-19 vaccine roll out.first six months of fiscal year 2022. 

 

Continuous Monitoring gross profit percentage increased eight percentage points and threenine percentage points for both the three and ninesix months ended December 31, 2020, respectively,September 30, 2021, primarily due to the reorganization of the business unit during the three months ended June 30, 2020, which has resulted in steady improvements to its operating efficiency as well as modifications made to our product offerings and pricing models which are intended to provide more predictable gross profit margins. 

Corporate and Other

Corporate and Other primarily consists of results from our Cold Chain Packaging division which was dissolvedwere implemented during the first quarter of fiscal year ended March 31, 20202021, and is no longer consideredto a reportable segment, as well as unallocated corporate expenses.lesser extent, the reorganization of the business during the first quarter of fiscal year 2021. 

  

Three Months Ended December 31,

  

Percentage

  

Nine Months Ended December 31,

  

Percentage

 
  2020  2019  Change  2020  2019  Change 
Revenues $-  $229   (100%) $-  $2,442   (100%)

Gross profit (loss)

  (140)  (18)  678%  (76)  395   (119%)

Gross profit (loss) as a % of revenues

  N/A   (8%)  N/A   N/A   16%  N/A 

Page 21

 

Operating Expenses

 

Operating expenses increased 13% for both the three and ninesix months ended December 31, 2020 increased 14% and 37%, respectively, asSeptember 30, 2021 compared to the prior year.three and six months ended September 30, 2020 as our overall business grew.

 

Selling

Selling expense is driven primarily by labor costs, including salaries and commissions; accordingly, it may vary with sales levels.

 

 

Three Months Ended December 31,

  

Percentage

  

Nine Months Ended December 31,

  

Percentage

  

Three Months Ended September 30,

  

Percentage

  

Six Months Ended September 30,

  

Percentage

 
 2020 2019 Change 2020 2019 Change  

2021

  

2020

  

Change

  

2021

  

2020

  

Change

 

Selling expense

 $4,753  $4,067  17% $12,614  $8,549  48% $4,643  $3,786  23% $9,501  $7,861  21%

As a percentage of revenues

 14% 13% 1% 13% 10% 3% 13% 12% 1% 13% 13% -%

 

Selling expense for the three and ninesix months ended December 31, 2020September 30, 2021 increased 17%23% and 48%21%, respectively, primarily as a result of selling costs incurred by the Biopharmaceutical Development division which we acquired and began consolidating into our results as of November 1, 2019 and unfavorable foreign exchange rates for selling expenses incurred in Swedish Krona, partially offset by lower professional services costs, lower commission costs, and lower travel-related costs as we implemented strict travel restrictions forexecuted on our previously-announced plan to invest in sales and marketing resources in order to increase organic revenues growth. Specifically, we hired several sales employees beginningduring the first quarter of fiscal year 2022, resulting in March, 2020.higher labor-related costs, including accruing commissions on higher sales. Further, we continued to invest in new marketing materials to support our sales staff. As a percentage of revenues, selling expense was 14%13% for both the three and six months ended December 31, 2020 and was 13% for the nine months ended December 31, 2020 asSeptember 30, 2021, compared to 13%12% and 10%13% for the three and ninesix months ended December 31, 2019,September 30, 2020, respectively. We plan to continue making modest, strategic investments in sales and marketing resources in order to further increase organic revenues growth. In addition, costs associated with the Biopharmaceutical Development division's sales force are expected to continue to result in higher selling expense as a percentage of revenues than we incurred historically; however, increases are expected to begin to normalize once the Biopharmaceutical Development division returns to normal sales levels.  In the near-term, we expect total selling expense will approximate 13% to approximate 10%-15%16% of revenues.revenues for fiscal year 2022.

 

General and Administrative

Labor costs including non-cash stock-based compensation, and amortization of intangible assets drive the substantial majority of our general and administrative expense.

 

 

Three Months Ended December 31,

  

Percentage

  

Nine Months Ended December 31,

  

Percentage

  

Three Months Ended September 30,

  

Percentage

  

Six Months Ended September 30,

  

Percentage

 
 2020 2019 Change 2020 2019 Change  

2021

  

2020

  

Change

  

2021

  

2020

  

Change

 

General and administrative expense

 $13,173  $11,605  14% $33,887  $26,806  26% $11,683  $10,615  10% $23,102  $20,714  12%

As a percentage of revenues

 39% 37% 2% 35% 32% 3% 33% 33% -% 33% 34% (1%)

 

General and administrative expenses increased 14%10% for the three monthsquarter ended December 31, 2020, primarilySeptember 30, 2021, as a result of:of increased amortization expense associated with intangible assets acquired fromsoftware costs as we implemented a new human resources information and payroll system during the GPT acquisition; three months ofquarter ended September 30, 2021, and unfavorable changes in foreign exchange rates, as general and administrative costs incurred byin Uppsala, Sweden are recorded in Swedish Krona and translated to USD for reporting purposes. Since the Biopharmaceutical Development divisionUSD has weakened against the Swedish Krona during the three monthsquarter ended December 31,September 30, 2021 as compared to the quarter ended September 30, 2020, versus only two months of expenses during the three months ended December 31, 2019; higher non-cash stock-based compensation expense, including the cumulative-effect true up for performance stock units recorded during the three months ended December 31, 2020; and higher professional services fees incurred for the implementation of our enterprise resource planning tool for GPT, partially offset by lower acquisition related costs.reported costs in USD have increased.

 

General and administrative expenses increased 26%12% for the ninesix months ended December 31, 2020 as a result of nine months of general and administrative costs incurred by the Biopharmaceutical Development division included in the results for the nine month period ended December 31, 2020 versus two months of results for the year to date period ended December 31, 2020 as the acquisition was completed on November 1, 2019.  Additionally, general and administrative costs increasedSeptember 30, 2021, primarily as a result of higher amortization expense associated with intangible assets acquired from the GPT acquisition, professional services fees related to the implementation of our enterprise resource planning tool for the division, and higher non-cash stock-based compensation expense, includingincreased amortization costs resulting from a $344 cumulative effect decrease to amortization expense recorded during the cumulative-effect true up for performance stock units recordedfirst quarter of fiscal year 2021 as part of a purchase price adjustment, increased software costs as we implemented a new human resources information and payroll system during the three months ended December 31, 2020, partially offset by lower acquisition related costs.September 30, 2021, and unfavorable change in foreign exchange rates. Our stock-based compensation expense increased in the six months ended September 30, 2021 primarily because we modified an RSU that resulted in recognition of compensation costs totaling $351 during the quarter ended June 30, 2021 and we issued restricted stock units in place of a portion of our executive team's cash bonuses and salaries, which were outstanding for a larger portion of the six months ended September 30, 2021 compared to the six months ended September 30, 2020. 

 

Page 2220


 

Research and Development

Research and development expense is predominantly comprised of labor costs and costs of third-party consultants.

 

 

Three Months Ended December 31,

  

Percentage

  

Nine Months Ended December 31,

  

Percentage

  

Three Months Ended September 30,

  

Percentage

  

Six Months Ended September 30,

  

Percentage

 
 2020 2019 Change 2020 2019 Change  

2021

  

2020

  

Change

  

2021

  

2020

  

Change

 

Research and development expense

 $2,705  $2,110  28% $7,715  $4,044  91% $2,613  $2,414  8% $5,424  $5,010  8%

As a percentage of revenues

 8% 7% 1% 8% 5% 3% 7% 8% (1%) 8% 8% -%

 

Research and development expenses increased 28% and 91%8% for the three and ninesix months ended December 31, 2020, respectively,September 30, 2021, primarily as a result of expenses attributable tothird-party contractor expenditures supporting our continued incremental investments in enhancing existing products as well as the Biopharmaceutical Development division, which we acquireddevelopment of new products and began consolidating into our resultsfeatures, as of November 1, 2019, and to a lesser extent because ofwell as unfavorable changes in foreign exchange rates on research and development expensesfor costs incurred in Swedish Krona. Including the Biopharmaceutical Development division, weUppsala, Sweden. We expect research and development expenses will be approximatelycontinue to approximate 7%-10% to 10% of revenues in the near term in part depending on the pace of the economic recovery.term. 

 

Nonoperating Expense 

 

  

Three Months Ended December 31,

  

Percentage Change

  

Nine Months Ended December 31,

  

Percentage

 
  2020  2019  2020 vs. 2019  2020  2019  Change 

Nonoperating expense

 $5,749   1,822   216% $10,651  $2,774   284%
  

Three Months Ended September 30,

  

Percentage

  

Six Months Ended September 30,

  

Percentage

 
  

2021

  

2020

  

Change

  

2021

  

2020

  

Change

 

Nonoperating (income) expense

 $(342)  2,086   (116%) $1,363  $4,902   (72%)

 

Nonoperating expense for the three and ninesix months ended December 31, 2020September 30, 2021 is composed primarily of interest expense and amortization of the debt discount associated with our 1.375% convertible senior notes issued indue August 201915, 2026 (the "Notes"), interest income earned on cash and cash equivalents, and gains and losses on foreign currency transactions.

 

During the three and nine months ended December 31, 2020, we incurred significant realized and unrealized foreign currency losses as a result of the USD weakening significantly, particularly against the Swedish Krona. 

Interest expense and amortization of debt discount was consistentdecreased for the three and six months ended December 31, 2020 compared to the three months ended December 31, 2019 and increased for nine months ended December 31, 2020 because the Note was outstanding for only part of the nine months ended December 31, 2019. Interest expense was offset primarily by interest income earned on our money market account. Higher interest was earned on the money market during the three and nine months ended December 31, 2019September 30, 2021 compared to the three and ninesix months ended December 31,September 30, 2020 as interest rates were higher in the prior year. 

As discussed in Note 1. within Item 1. Financial Statements, subsequentdue to theour adoption of Accounting Standards UpdateASU 2020-06, there will bewhich resulted in a reduction in non-cash interest expense related to the 1.375% convertible seniorNotes. Nonoperating expenses also decreased as we recorded net unrealized gains on foreign currency related to certain of our intercompany notes due August 15, 2025.resulting from the movement of the Swedish Krona against the USD.

 

Income Taxes

 

 

Three Months Ended December 31,

  

Percentage Change

  

Nine Months Ended December 31,

  

Percentage

  

Three Months Ended September 30,

  

Percentage

  

Six Months Ended September 30,

  

Percentage

 
 2020 2019 2020 vs. 2019 2020 2019 Change  

2021

  

2020

  

Change

  

2021

  

2020

  

Change

 

Income tax (benefit) expense

 $(1,185) $(573) 107% $(1,943) $792  (345%)

Income tax provision (benefit)

 $823  $(295) (379%) $246  $(758) (132%)

Effective tax rate

 21% 11% 10% 75% 19% 56% 18% (12%) 30% 4% (24%) 28%

 

Our effective tax rate benefited notably from the release of an uncertain tax position of $630, the exercise of stock options and to a lesser extent, lower pre-tax income.the benefit of federal derived intangible income, partially offset by the limitations imposed by Section 162(m) and higher state income taxes. Our income tax rate varies based upon many factors, but in general, we anticipate that on a go-forward basis our effective tax rate as adjusted for the GPT Acquisition will be approximately 25%26%, plus or minus the impact of excess tax benefits and deficiencies associated with share-based payment awards to employees; see Note 10.9. “Income Taxes” within Item 1. Financial Statements for additional discussion. The excess tax benefits and deficiencies associated with share-based payment awards to our employees have caused and, in the future, may cause large fluctuations in our realized effective tax rate based on timing, volume, and nature of stock options exercised under our share-based payment program.

 

Net (Loss) Income 

Net (loss)income for the ninesix months ended December 31, 2020September 30, 2021 varied with the changes in revenues, gross profit, and operating expenses (which(and includes $6,887, $10,694,$7,573 and $4,024$4,236 of non-cash: stock-based compensation,non-cash amortization of intangible assets acquired in a business combination, and stock-based compensation, respectively). Prior to the adoption of ASU 2020-06 on April 1, 2021, we were required to recognize non-cash interest expense related to the amortization of debt discounts and discountissuance costs. Subsequent to the adoption, we recognize non-cash interest expense related to amortization onof debt issuance costs only, resulting in higher net income subsequent to the Notes, respectively, partially offset by a $436 benefit associated with a cumulative effect true upadoption of inventory step up amortization).ASU 2020-06. 

Page 23

 

Liquidity and Capital Resources

 

Our sources of liquidity include cash generated from operations, cash and cash equivalents on hand, working capital and potential additional equity and debt offerings. Despite lingering uncertainties surrounding the economic impacts of the COVID-19 pandemic, we continue to believe that we have the liquidity required to continue operations even if volatility in the economic environment reoccurs. We believe that cash and cash equivalents on hand and cash generated from operations, as well as the reminder of the unused capacity under our Credit Facility will be sufficient to meet our short-term and long-term needs.

Our more significant uses of resources have historically included acquisitions, long-term capital expenditures, payment of debt and interest obligations, and quarterly dividends to shareholders. Although the COVID-19 pandemic has resulted in lower revenues overall, we continue to believe that we have the liquidity required to continue operations during this volatile period. During the nine months ended December 31, 2020, we took steps to reduce cash outlays and expenses, including limiting travel, reducing hiring new employees, and converting a portion of our executives' remuneration from cash to non-cash stock-based compensation incentives. 

Even given current macroeconomic conditions, we believe that cash and cash equivalents on hand and cash generated from operations will be sufficient to meet our short-term and long-term needs. Additionally, we believe that we have access to equity and credit markets if necessary. However, additional equity or debt financing, or other transactions, may not be available on acceptable terms, if at all.  

Working capital is the amount by which current assets exceed current liabilities. We had working capital of $267,525$290,714 and $96,784 at December 31, 2020,$271,166 as of September 30, 2021, and March 31, 2020,2021, respectively. As of December 31, 2020,September 30, 2021, and March 31, 2020,2021, we had $253,731$278,294 and $81,380,$263,865, respectively, of cash and cash equivalents, which were held primarily in money market funds. We consider all highly liquid investments with an original maturity of three months or less when purchased to be cash equivalents.

Page 21

During fiscal year 2021, we entered into a four-year senior secured credit agreement that includes 1) a revolving credit facility in an aggregate principal amount of up to $75,000, 2) a swingline loan in an aggregate principal amount not exceeding $5,000, and 3) letters of credit in an aggregate stated amount not exceeding $2,500 at any time. The Credit Facility also provides for an incremental term loan or an increase in revolving commitments in an aggregate principal amount of at a minimum $25,000 and at a maximum $75,000, subject to the satisfaction of certain conditions and lender considerations. As of September 30, 2021, we had not drawn from the Credit Facility. 

 

On June 9, 2020,October 20, 2021, we completed the saleacquisition of Agena for $300,000, subject to customary purchase price adjustments, pursuant to the terms of the previously announced Agreement and issuancePlan of 600,000 shares of our common stockMerger dated September 13, 2021. We funded the acquisition and transactions relating thereto with cash on hand, and on June 16, 2020,October 18, 2021, we drew $70,000 on our underwriters exercised in full their optionexisting line of credit for cash funds necessary to purchase an additional 90,000 sharescomplete the acquisition. Following the draw, we had $5,000 remaining available to draw on the line of our common stock. The offering price to the public was $225.00 per share. The total proceeds we received from the offering, net of underwriting discounts and commissions and other offering expenses that we initially paid was $145,935.credit.  

 

As of December 31, 2020,September 30, 2021, $172,500 in aggregate principal amount Notes was outstanding. The Notes bear interest at a rate of 1.375% payable semi-annually in arrears on February 15 and August 15 of each year, beginning with our first payment made on February 15, 2020. These Notes can be converted by holders prior to maturity if certain conditions are met. We currently expect to settle future conversions of the Notes entirely in shares of our common stock and will reevaluate this policy from time to time in the event that conversion conditions are met and conversion notices are received from holders of the Notes. We were in compliance with all debt agreements at December 31, 2020September 30, 2021 and for all prior years presented and have met all debt payment obligations. Refer to Note 7.6. "Indebtedness" within Item 1. Financial Statements for more details on these transactions. 

We routinely evaluate opportunities for strategic acquisitions. Future material acquisitions may require that we obtain additional capital, assume additional third-party debt or incur other long-term obligations. We believe that we have the ability to issue more equity or debt in the future in order to finance our acquisition and investment activities, however, additional equity or debt financing, or other transactions, may not be available on acceptable terms, if at all.

We may from time to time repurchase or otherwise retire our debt and take other steps to reduce our debt or otherwise improve our balance sheet.debt. These actions may include retirements or refinancing of outstanding debt, privately negotiated transactions or otherwise. The amount of debt that may be retired, if any, could be material and would be decided at the sole discretion of our Board of Directors and will depend on market conditions, our cash position and other considerations.

 

We routinely evaluate opportunities for strategic acquisitions. We currently have significant cash and cash equivalents on hand, but future material acquisitions may require that we obtain additional capital, assume additional third-party debt or incur other long-term obligations. We believe that we have the ability to issue more equity or debt in the future in order to finance our acquisition and investment activities.

Dividends

 

We have paid regular quarterly dividends since 2003. We declared and paid dividends of $0.16 per share during each of the nine monthsquarters ended December 31, 2020June 30, 2021 and September 30, 2021, as well as each quarter for theof fiscal year ended March 31, 2020.2021.

 

In JanuaryOctober 2021, we announced that our Board of Directors declared a quarterly cash dividend of $0.16 per share of common stock, payable on MarchDecember 15, 2021, to shareholders of record at the close of business on February 26,November 30, 2021.

Page 24

 

Cash Flows

 

Our cash flows from operating, investing, and financing activities were as follows (in thousands):

 

 

Nine Months Ended December 31,

  

Six Months Ended September 30,

 
 

2020

  

2019

  

2021

  

2020

 

Net cash provided by operating activities

 $23,553  $18,156  $14,023  $12,610 

Net cash (used in) investing activities

 (954) (185,037) (1,591) (707)

Net cash provided by financing activities

 147,275  230,883  1,423  147,104 

 

Cash flows from operating activities for the ninesix months ended December 31, 2020September 30, 2021 provided $23,553, which$14,023.  The $1,413 increase in cash flows from operations primarily resulted from increased net income and and increased non-cash stock-based compensation expense, partially offset by lower depreciation and amortization and lower non cash providedinterest expense as a result of the adoption of ASU 2020-06.  Further, cash used by GPT's operationsoperating assets and favorable changes in our working capital accounts.liabilities decreased by $887 for the six months ended September 30, 2021 compared to the six months ended September 30, 2020. Cash used in investing was lowerhigher during the ninesix months ended December 31, 2020September 30, 2021 compared to the ninesix months ended December 31, 2019, which included a cash outlay forSeptember 30, 2020, due to purchases of property, plant, and equipment, primarily to support the IBP and GPT acquisitions. Cash provided by financing activities includedrenovations of our Lakewood, Colorado facility. Our equity raise which provided $145,935completed during the nine monthsquarter ended December 31,June 30, 2020 and our convertible debt offering and equity raise which provided $252,065 during the nine months ended December 31, 2019. $145,935.

 

Page 22

Contractual Obligations and Other Commercial Commitments

 

We are party to many contractual obligations that involve commitments to make payments to third parties in the ordinary course of business. For a description of our contractual obligations and other commercial commitments as of March 31, 2020,2021, see our Form 10-K for the fiscal year ended March 31, 2020,2021, filed with the Securities and Exchange Commission on June 1, 2020.2021. During the ninethree and six months ended December 31, 2020,September 30, 2021, there were no material changes with respect to the nature of our contractual obligations and other commercial commitments outside the ordinary course of business. At December 31, 2020,September 30, 2021, we had contractual obligations for open purchase orders of approximately $6,610$11,099 for routine purchases of supplies and inventory, which are payable in less than one year. Open purchase orders increased during the three months ended September 30, 2021 as we took proactive steps to mitigate risks in our supply by increasing our orders of certain critical raw materials.  

 

Off-Balance Sheet Arrangements

 

As of December 31, 2020,September 30, 2021, we had no off-balance sheet arrangements or obligations.

 

Critical Accounting Policies and Estimates

 

Critical accounting estimates are those that we believe are both significant and require us to make difficult, subjective, or complex judgments, often because we need to estimate the effect of inherently uncertain matters. These estimates are based on historical experience and various other factors that we believe to be appropriate under the circumstance. Actual amounts and results could differ from these estimates made by management. Certain accounting policies that require significant management estimates and are deemed critical to our results of operations or financial position are discussed in our Annual Report on Form 10-K for the year ended March 31, 2020,2021, in the Critical Accounting Policies and Estimates section of “ItemItem 7. Management's Discussion and Analysis of Financial Condition and Results of Operations.”Operations.

 

Item 3. Quantitative and Qualitative Disclosures about Market Risk

 

We have no derivative instruments and minimal exposure to commodity market risks. Our reporting currency is U.S. dollars, and the functional currency of each of our foreign subsidiaries is its respective local currency. Our operations include activities outside of the U.S. and we have currency risk on the transactions in other currencies and translation adjustments resulting from the conversion of our international financial results into the U.S. dollar. We face currency exposures in our global operations as a result of various factors including intercompany currency denominated loans, selling our products in various currencies, purchasing raw materials and equipment in various currencies and tax exposures not denominated in the functional currency. These exposures have increased as a resultwe have continued to expand internationally, including the acquisition of the GPT, Acquisition, which conducts a substantial portion of its business expenses in Swedish Krona. Fluctuations in exchange rates have, and may continue to adversely affect our results of operations, financial position, and cash flows.flows; however we do not believe a 10% adverse change in currency would materially affect our consolidated results. 

 

We hold investments in money market funds. As a result, we are exposed to potential loss from market risks that may occur as a result of changes in interest rates, credit quality of the issuer, or other factors. 

 

Page 25

Item 4. Controls and Procedures

 

Evaluation of Disclosure Controls and Procedures

We maintain disclosure controls and procedures (as defined in RulesRule 13a-15(e) and 15d-15(e) promulgated under the Securities Exchange Act of 1934, as amended (the “Exchange Act”) that are designed to ensure that information required to be disclosed in Exchange Act reports is recorded, processed, summarized and reported within the time periods specified in the Securities and Exchange Commission’s rules and forms, and that such information is accumulated and communicated to our management, including our principal executiveChief Executive Officer and principal financial officers, or persons performing similar functions,Chief Financial Officer, as appropriate, to allow timely decisions regarding required disclosure.

 

Evaluation of Disclosure Controls and Procedures

As of December 31, 2020,September 30, 2021, we carried out an evaluation, under the supervision and with the participation of our management, including our chief executive officerChief Executive Officer and chief financial officer,Chief Financial Officer, of the effectiveness of the design and operation of our disclosure controls and procedures. Our chief executive officerBased on the foregoing, our Chief Executive Officer and chief financial officerChief Financial Officer concluded that our disclosure controls and procedures were effective as of the end of the period covered by this report, given the remediation of the material weakness described in more detail below.report.

 

Remediation of Material Weakness

As disclosed in Part II Item 9A. "Controls and Procedures" in our annual report on Form 10-K for the year ended March 31, 2020, during the three months ended March 31, 2020, we identified a material weakness in internal controls related to ineffective information technology general controls ("ITGCs") in the areas of user access and program change management over certain information technology ("IT") systems that support our financial reporting processes. 

Beginning during the three months ended March 31, 2020, and continuing through June 30, 2020, we implemented our previously-disclosed remediation plan that included: (i) training programs addressing ITGCs and policies around internal controls over financial reporting, which included educating control owners concerning the requirements of each control that they are responsible for; (ii) creation of roles that are responsible for IT compliance and oversight; (iii) development of documentation underlying ITGCs to promote knowledge transfer upon personnel and function changes; (iv) an IT management review and testing plan to monitor ITGCs with a specific focus on systems supporting our financial reporting processes; and (v) enhanced quarterly reporting on the remediation measures to the Audit Committee of the Board of Directors.

During the three months ended June 30, 2020, we completed our testing of the operating effectiveness of the affected ITGC controls and found them to be effective. As a result, we have concluded that the material weakness was remediated as of June 30, 2020 and our disclosure controls and procedures were effective as of December 31, 2020.  

Changes in Internal Control over Financial Reporting

The GPT Acquisition was completed on October 31, 2019, and the financial results of GPT are included in our unaudited consolidated financial statements as of December 31, 2020 and for the period then ended. During the time since acquisition,three months ended September 30, 2021, we have assessed the control environment of GPT, made certain changes to GPT's internal controls over financial reporting, including design changes that were required as we brought GPT onto our enterprise resource planning tool,implemented a new human resources information and we have performed testing over the operating effectiveness of many of GPT's internal controls. We now consider GPTpayroll system, which is considered to be included in the scopea key system as part of our assessment of internal controls over financial reporting. 

We continued to integrate the software with our processes, systems, and controls in the quarter ended September 30, 2021.  There were no other changes during the quarter ended September 30, 2021 in our internal control over financial reporting (as defined in Rule 13a-15(f) under the Exchange Act) that have materially affected or are reasonably likely to materially affect our internal control over financial reporting. 

 

Page 2623


 

Part II. Other Information

 

Item 1. Legal Proceedings

 

See Note 11.10. “Commitments and Contingencies” within Item 1. Financial Statements.Statements for information regarding any legal proceedings in which we may be involved.

 

Item 1A. Risk factors

 

We are affecteddependent on oursuppliers to deliver components, and a shortage of key components have and could continue to disrupt our production and delay order fulfillment.

Products sold by risks specificour Instruments division, and to usa lesser extent, our Biopharmaceutical Development, and Continuous Monitoring divisions contain components, including electronic components, glass, plastics, and packaging that we source globally from suppliers who, in turn, source components from their suppliers. If there is a shortage of a key component in our supply chain, and the component cannot be easily sourced from a different supplier, the shortage may disrupt our production which may, in turn, delay order fulfillment.  We are experiencing long lead times, and in some cases, difficulty obtaining components from our existing suppliers, which has resulted in delayed order fulfillment in our Instruments division.  In addition, costs for components, and freight for components has increased, which may reduce our gross profit margins until we are able to pass the cost increases along to our customers. There are several reasons for the supply chain disruptions to components that we rely on to manufacture our products including: increased demand for other products that use the same components as well as factorsthose we purchase, manufacturing shut-downs during the past 18 months that affect all businesses operatingreduced production of components, labor issues, and long lead times for raw materials used in the production of components.  A continued shortage of components or other key materials that comprise the components could cause a global market.  The significant factors knowndisruption to us that could materially adversely affect our business,production schedule and have a substantial adverse effect on our financial condition or operating results areof operations.

Additional risks related to our supply chain include those in our FY21 Form10-K risk factors, “We face numerous manufacturing and supply chain risks. In addition, our reliance upon sole or limited sources of supply for certain materials, components and services could cause production interruptions, delays and inefficiencies.

During the quarter there were no other material changes from the risk factors described in Item 1A. Risk Factors of our Annual Report on Form 10-K for the year ended March 31, 2020, under the heading “Risk Factors” in Part I – Item 1A.  Information regarding risk factors also appears in “Management’s Discussion and Analysis of Financial Condition and Results of Operations – Forward Looking Statements” in Part I - Item 2 of this Form 10-Q.  The Risk Factors section in our Annual Report on Form 10-K for the year ended March 31, 2020, as updated by this Form 10-Q including the discussions in “Management’s Discussion and Analysis of Financial Condition and Results of Operations –Business Overview—COVID-19 and Business Update”, remains current in all material respects. These risk factors do not identify all risks that we face—our operations could also be affected by factors that are not presently known to us or that we currently consider to be immaterial to our operations. Due to risks and uncertainties, known and unknown, our past financial results may not be a reliable indicator of future performance and historical trends should not be used to anticipate results or trends in future periods.2021. 

 

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds

 

On November 7, 2005, our Board of Directors adopted a share repurchase plan which allows for the repurchase of up to 300,000 of our common shares, of which 162,486 have been purchased to date; however, no shares have been purchased under the plan in the last three fiscal years. This plan will continue until the maximum is reached or the plan is terminated by further action of the Board of Directors. 

 

Page 2724


 

Item 6. Exhibits

 

Exhibit No.

Description of Exhibit

10.2.3Mesa Laboratories, Inc. 2021 Equity Incentive Plan (incorporated by reference from exhibit 10.2.3 to Mesa Laboratories, Inc.'s Form S-8 filed on August 30, 2021 (Commission File Number: 333-259154)
10.3.7Form of 2021 Equity Incentive Plan Option Award Agreement (incorporated by reference from exhibit 10.3.7 to Mesa Laboratories, Inc.'s Form S-8 filed on August 30, 2021 (Commission File Number: 333-259154)
10.3.8Form of 2021 Equity Incentive Plan Restricted Stock Unit Agreement (incorporated by reference from exhibit 10.3.8 to Mesa Laboratories, Inc.'s Form S-8 filed on August 30, 2021 (Commission File Number: 333-259154)

31.1+

Certification of Chief Executive Officer Pursuant to Section 302 of the Sarbanes-Oxley Act of 2002

31.2+

Certification of Chief Financial Officer Pursuant to Section 302 of the Sarbanes-Oxley Act of 2002

32.1*

Certification of Chief Executive Officer Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002

32.2*

Certification of Chief Financial Officer Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002

101.INS+XBRL Instance Document - the instance document does not appear in the Interactive Data File because its XBRL tags are embedded within the Inline XBRL document.
101.SCH+Inline XBRL Taxonomy Extension Schema Docment.Document.
101.CAL+Inline XBRL Taxonomy Extension Calculation Linkbase Document
101.DEF+Inline XBRL Taxonomy Extension Definitions Linkbase Document
101.LAB+Inline XBRL Taxonomy Extension Label Linkbase Document
101.PRE+Inline XBRL Taxonomy Extension Presentation Linkbase Document

104+

Cover Page Interactive Data File (formatted as Inline XBRL with applicable taxonomy extension information contained in Exhibits 101.*).

 



+ Filed herewith

* Furnished herewith

 

Page 2825


 

Signatures

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

 

 

MESA LABORATORIES, INC.

(Registrant)

 

 

DATED: February 3,November 4, 2021BY:

/s/ Gary M. Owens.

Gary M. Owens

Chief Executive Officer

   
   
DATED: February 3,November 4, 2021BY:

/s/ John V. Sakys

John V. Sakys

Chief Financial Officer

                       

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