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WARNING LETTER
•FELLA GROUP LLC•December 10, 2021

FELLA GROUP LLC – FDA Warning Letter, Dec 10, 2021

Record Details

On February 25, 2022, the FDA issued a Warning Letter to FELLA GROUP LLC following a Foreign Supplier Verification Programs (FSVP) inspection on December 10, 2021, and a previous inspection on July 28, 2020. The inspections aimed to assess compliance with section 805 of the FD&C Act and 21 CFR part 1 subpart L, which mandate risk-based activities for importers to verify that imported food meets U.S. food safety standards.

The FDA found significant violations, specifically that FELLA GROUP LLC did not develop, maintain, and follow an FSVP for imported foods, as required by 21 CFR 1.502(a). This non-compliance was noted despite a previous commitment in response to the July 2020 inspection to develop an FSVP plan by July 31, 2021. A subsequent response dated January 6, 2022, again stated a plan to develop an FSVP by December 15, 2022, but adequate corrective actions or sufficient FSVP documentation have not been provided.

Failure to address these violations may result in further FDA action, including refusal of admission for imported food under section 801(a)(3) of the FD&C Act, and placement on detention without physical examination (DWPE) via Import Alert #

Company
FELLA GROUP LLC
Inspection date
December 10, 2021
Product type
Food
Office
Division of West Coast Imports
Person
  • Kathleen Turner (Program Division Director)
View Company Profile

ID · b96ceea0-c5ec-4545-81a0-42a9b5142a10

Violation Codes7
21 U.S.C. 384aFD&C Act 80521 CFR 1.502(a)FD&C Act 801(a)(3)21 U.S.C. 381(a)(3)FD&C Act 301(zz)21 U.S.C. 331(zz)

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