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WARNING LETTER
•A&M; Farms•January 5, 2012

A&M; Farms – FDA Warning Letter, Jan 5, 2012

Record Details

On January 4 and 5, 2012, the FDA inspected A&M Farms in Fresno, California, and found violations of the Federal Food, Drug, and Cosmetic Act. A cow consigned for slaughter on September 30, 2011, was found to have penicillin at 0.12 ppm in kidney tissue, exceeding the 0.05 ppm tolerance, rendering the food adulterated under 21 U.S.C. § 342(a)(2)(C)(ii).

The investigation also revealed insanitary conditions, specifically a failure to maintain complete treatment records, indicating that medicated animals with harmful drug residues are likely to enter the food supply, thus adulterating food under 21 U.S.C. § 342(a)(4).

Furthermore, A&M Farms adulterated the new animal drug (b)(4) brand (b)(4) (penicillin G procaine) Injectable Suspension by using it extralabel without following approved dosage amounts and per-injection site guidelines. This extralabel use was not under the supervision of a licensed veterinarian, violating 21 C.F.R. 530.11(a), and resulted in an illegal drug residue, violating 21 C.F.R. 530.11(d). This caused the drug to be unsafe and adulterated under 21 U.

Company
A&M; Farms
Inspection date
January 5, 2012
Product type
Drugs
Office
Department of Health and Human Services
Person
  • Barbara J. Cassens (Director )
View Company Profile

ID · 7367ea86-ce8f-43d1-b7b6-76a8a6b85406

Violation Codes10
21 U.S.C. 342(a)(2)(C)(ii)21 U.S.C. 360b21 U.S.C. 342(a)(4)21 CFR 556.51021 CFR 530.3(a)21 U.S.C. 360b(a)(4)21 U.S.C. 360b(a)(5)21 CFR 530.11(a)21 CFR 530.11(d)21 U.S.C. 360b(a)

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