FDA Inspection 987944 — Glick, Amos

Glick, Amos — FEI 3012423450

The FDA completed an inspection of Glick, Amos on October 7, 2016 in Drumore, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 7, 2016
Fiscal Year
2017
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Drumore, PA (United States)

Citations

IDCFRDescription
409321 CFR 530.11(d)ELDU - producer causes Illegal drug residue
4182FDCA 501(a)(5)ELDU without veterinary client-patient relationship
4185FDCA 402(a)(4)Record keeping