FDA Inspection 697798 — Huvepharma Inc.

Huvepharma Inc. — FEI 2316679

The FDA completed an inspection of Huvepharma Inc. on November 16, 2010 in Van Buren, AR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 16, 2010
Fiscal Year
2011
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Van Buren, AR (United States)

Citations

IDCFRDescription
429721 CFR 226.42(a)Components receiving, testing, handling, et. al.