FDA Inspection 1071522 — Animart, Inc.

Animart, Inc. — FEI 2129513

The FDA completed an inspection of Animart, Inc. on November 13, 2018 in Beaver Dam, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 13, 2018
Fiscal Year
2019
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Beaver Dam, WI (United States)

Citations

IDCFRDescription
1352121 CFR 530.41(a)Drugs prohibited for extralabel use in food-producing animal(s)
409721 CFR 530.20(a)(2)(iv)Prescribed ELDU - vet causes an illegal drug residue