FDA Inspection 1031592 — Bimeda, Inc.

Bimeda, Inc. — FEI 2110168

The FDA completed an inspection of Bimeda, Inc. on November 17, 2017 in Le Sueur, MN. 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 17, 2017
Fiscal Year
2018
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Le Sueur, MN (United States)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
179021 CFR 211.80(b)Handling and Storage to Prevent Contamination