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SEC Comment Letter 0000000000-23-011972 to Fulgent Genetics, Inc. (FLGT) (CIK 0001674930) (FLGT)

Fulgent Genetics, Inc. (FLGT) (CIK 0001674930)
Date: Nov. 1, 2023 · CIK: 0001674930 · Accession: 0000000000-23-011972

AI Filing Summary & Sentiment

File numbers found in text: 001-37894

Date
November 1, 2023
Author
Not clearly detected
Form
UPLOAD
Company
Fulgent Genetics, Inc. (FLGT) (CIK 0001674930)

Letter

United States securities and exchange commission logo November 1, 2023 Paul Kim Chief Financial Officer Fulgent Genetics, Inc. 4399 Santa Anita Avenue El Monte, California 91731 Re:Fulgent Genetics, Inc. Form 10-K for Fiscal Year Ended December 31, 2022 Filed February 28, 2023 File No. 001-37894 Dear Paul Kim: We have limited our review of your filing to the financial statements and related disclosures and have the following comment(s). Please respond to this letter within ten business days by providing the requested information or advise us as soon as possible when you will respond. If you do not believe a comment applies to your facts and circumstances, please tell us why in your response. After reviewing your response to this letter, we may have additional comments. Form 10-K for Fiscal Year Ended December 31, 2022 Item 7. Management's Discussion and Analysis of Financial Condition and Results of Operations Results of Operations, page 54 1.We note that the significant decline in COVID-19 testing revenues has significantly impacted your results of operations for fiscal year 2022. As these revenues are not anticipated to be a material part of your ongoing results of operations, please provide an analysis of the material factors that impact the revenues that are expected to be a material part of your results of operations going forward in comparison to the corresponding revenues for the prior period. Also provide a discussion and analysis of the material factors impacting the associated gross profit for these revenues to provide investors with a better understanding of your future expectations of your operating results with the remaining primary diagnostic testing revenues. When multiple factors are discussed, quantify the extent to which each factor impacted the related operating result line items. Refer to Item 303(b)(2) of Regulation S-K and Section 501.12 of the Financial Reporting Codification for guidance.

FirstName LastNamePaul Kim Comapany NameFulgent Genetics, Inc. November 1, 2023 Page 2 FirstName LastNamePaul Kim Fulgent Genetics, Inc. November 1, 2023 Page 2 2.We note that you incur research and development expenses related to your diagnostics testing business and for your therapeutics development business. Please expand your discussion and analysis to quantify the costs for each of your research and development projects and to discuss the nature of the costs incurred for each project. Critical Accounting Policies and Use of Estimates Valuation of Goodwill and Intangible Assets, page 59 3.We note that you recognized $143 million of goodwill and $64.6 million of IPR&D, an indefinite-lived intangible asset, as of December 31, 2022. Please provide a more comprehensive discussion and analysis of the critical estimates associated with assessing goodwill and the indefinite-lived intangible asset for impairment. In this regard, we note that the fourth quarter of fiscal year 2022 is the first time you recognized operating and net losses since the second quarter of fiscal year 2020 due to the significant decline in revenues from COVID-19 testing. Expanded disclosures are to provide investors with sufficient information to assess any material uncertainty regarding the realizability of goodwill and the indefinite-lived intangible asset, including but not limited to the following. •The percentage by which the estimated fair value exceeds the carrying value of your reporting unit(s) or indefinite-lived intangible asset to the extent that the fair value does not substantially exceed the carrying value. •The methodologies used to estimate the fair value of the reporting unit(s) and the indefinite-lived intangible asset for the most recent quantitative assessment, including the material judgements, assumptions and estimates made. •A discussion of the degree of uncertainty associated with the key assumptions and estimates along with the potential impact reasonably possible changes in the key assumptions would have on your impairment analysis. •A discussion of the potential events and/or changes in circumstances that could reasonably be expected to occur and negatively affect the key assumptions and result in a material impairment charge. Refer to Item 303(b)(3) of Regulation S-K and Section 501.14 of the Financial Reporting Codification for guidance. Note 2. Summary of Significant Accounting Policies Goodwill, page F-13 4.Please expand your accounting policy to disclose the level at which you are testing goodwill for impairment (i.e., the identification of your reporting unit(s)). Also disclose when you perform your annual impairment test, the circumstances in which you would perform an interim impairment test, and the method(s) used to estimate the fair value of your reporting unit(s) to the extent that you prepare a quantitative assessment. Reporting Segment and Geographic Information, page F-15 5.We note your disclosure that you view your operations and manage your business in one

FirstName LastNamePaul Kim Comapany NameFulgent Genetics, Inc. November 1, 2023 Page 3 FirstName LastName Paul Kim Fulgent Genetics, Inc. November 1, 2023 Page 3 “reporting segment”. We further note that you acquired Fulgent Pharma, a clinical-stage, therapeutics development company, which differs from your historical clinical diagnostic business. As such, please tell us your consideration of the guidance in ASC 280-10-50-1 through 50-5 for the identification of your operating segments and/or reportable segments. Note 15. Business Combinations Fulgent Pharma Holdings, Inc, page F-33 6.We note that you acquired Fulgent Pharma with one drug candidate for which IPR&D of $64.6 million was recognized compared to the purchase price of $68 million. Please address each of the following: •Provide us with your analysis of the guidance in ASC 805-10-55-5A through 55-5C, including the calculation of the screen test. •To the extent that you are able to demonstrate the screen test is not met, provide us with your analysis of Fulgent Pharma meeting the definition of a business based on the guidance in ASC 805-10-55. In closing, we remind you that the company and its management are responsible for the accuracy and adequacy of their disclosures, notwithstanding any review, comments, action or absence of action by the staff. Please contact Tracey Houser at 202-551-3736 or Terence O'Brien at 202-551-3355 with any questions. Sincerely, Division of Corporation Finance Office of Industrial Applications and Services

Show Raw Text
United States securities and exchange commission logo
November 1, 2023
Paul Kim
Chief Financial Officer
Fulgent Genetics, Inc.
4399 Santa Anita Avenue
El Monte, California 91731
Re:Fulgent Genetics, Inc.
Form 10-K for Fiscal Year Ended December 31, 2022
Filed February 28, 2023
File No. 001-37894
Dear Paul Kim:
            We have limited our review of your filing to the financial statements and related
disclosures and have the following comment(s).
            Please respond to this letter within ten business days by providing the requested
information or advise us as soon as possible when you will respond. If you do not believe a
comment applies to your facts and circumstances, please tell us why in your response.
            After reviewing your response to this letter, we may have additional comments.
Form 10-K for Fiscal Year Ended December 31, 2022
Item 7. Management's Discussion and Analysis of Financial Condition and Results of Operations
Results of Operations, page 54
1.We note that the significant decline in COVID-19 testing revenues has significantly
impacted your results of operations for fiscal year 2022.  As these revenues are not
anticipated to be a material part of your ongoing results of operations, please provide an
analysis of the material factors that impact the revenues that are expected to be a material
part of your results of operations going forward in comparison to the corresponding
revenues for the prior period.  Also provide a discussion and analysis of the material
factors impacting the associated gross profit for these revenues to provide investors with a
better understanding of your future expectations of your operating results with the
remaining primary diagnostic testing revenues.  When multiple factors are discussed,
quantify the extent to which each factor impacted the related operating result line items.
Refer to Item 303(b)(2) of Regulation S-K and Section 501.12 of the Financial Reporting
Codification for guidance.

 FirstName LastNamePaul Kim
 Comapany NameFulgent Genetics, Inc.
 November 1, 2023 Page 2
 FirstName LastNamePaul Kim
Fulgent Genetics, Inc.
November 1, 2023
Page 2
2.We note that you incur research and development expenses related to your diagnostics
testing business and for your therapeutics development business.  Please expand your
discussion and analysis to quantify the costs for each of your research and development
projects and to discuss the nature of the costs incurred for each project.
Critical Accounting Policies and Use of Estimates
Valuation of Goodwill and Intangible Assets, page 59
3.We note that you recognized $143 million of goodwill and $64.6 million of IPR&D, an
indefinite-lived intangible asset, as of December 31, 2022.  Please provide a more
comprehensive discussion and analysis of the critical estimates associated with assessing
goodwill and the indefinite-lived intangible asset for impairment.  In this regard, we note
that the fourth quarter of fiscal year 2022 is the first time you recognized operating and
net losses since the second quarter of fiscal year 2020 due to the significant decline in
revenues from COVID-19 testing.  Expanded disclosures are to provide investors with
sufficient information to assess any material uncertainty regarding the realizability of
goodwill and the indefinite-lived intangible asset, including but not limited to the
following.
•The percentage by which the estimated fair value exceeds the carrying value of your
reporting unit(s) or indefinite-lived intangible asset to the extent that the fair value
does not substantially exceed the carrying value.
•The methodologies used to estimate the fair value of the reporting unit(s) and the
indefinite-lived intangible asset for the most recent quantitative assessment, including
the material judgements, assumptions and estimates made.
•A discussion of the degree of uncertainty associated with the key assumptions and
estimates along with the potential impact reasonably possible changes in the key
assumptions would have on your impairment analysis.
•A discussion of the potential events and/or changes in circumstances that could
reasonably be expected to occur and negatively affect the key assumptions and result
in a material impairment charge.
Refer to Item 303(b)(3) of Regulation S-K and Section 501.14 of the Financial Reporting
Codification for guidance.
Note 2. Summary of Significant Accounting Policies
Goodwill, page F-13
4.Please expand your accounting policy to disclose the level at which you are testing
goodwill for impairment (i.e., the identification of your reporting unit(s)).  Also disclose
when you perform your annual impairment test, the circumstances in which you would
perform an interim impairment test, and the method(s) used to estimate the fair value of
your reporting unit(s) to the extent that you prepare a quantitative assessment.
Reporting Segment and Geographic Information, page F-15
5.We note your disclosure that you view your operations and manage your business in one

 FirstName LastNamePaul Kim
 Comapany NameFulgent Genetics, Inc.
 November 1, 2023 Page 3
 FirstName LastName
Paul Kim
Fulgent Genetics, Inc.
November 1, 2023
Page 3
“reporting segment”.  We further note that you acquired Fulgent Pharma, a clinical-stage,
therapeutics development company, which differs from your historical clinical diagnostic
business.  As such, please tell us your consideration of the guidance in ASC 280-10-50-1
through 50-5 for the identification of your operating segments and/or reportable segments.
Note 15. Business Combinations
Fulgent Pharma Holdings, Inc, page F-33
6.We note that you acquired Fulgent Pharma with one drug candidate for which IPR&D of
$64.6 million was recognized compared to the purchase price of $68 million.  Please
address each of the following:
•Provide us with your analysis of the guidance in ASC 805-10-55-5A through 55-5C,
including the calculation of the screen test.
•To the extent that you are able to demonstrate the screen test is not met, provide us
with your analysis of Fulgent Pharma meeting the definition of a business based on
the guidance in ASC 805-10-55.
            In closing, we remind you that the company and its management are responsible for the
accuracy and adequacy of their disclosures, notwithstanding any review, comments, action or
absence of action by the staff.
            Please contact Tracey Houser at 202-551-3736 or Terence O'Brien at 202-551-3355 with
any questions.
Sincerely,
Division of Corporation Finance
Office of Industrial Applications and
Services