FDA Inspection 632163 — Huvepharma Inc.

Huvepharma Inc. — FEI 1931473

The FDA completed an inspection of Huvepharma Inc. on Dec 2, 2009 in Saint Joseph, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 2, 2009
Fiscal Year
2010
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Saint Joseph, MO (United States)

Citations

IDCFRDescription
434221 CFR 211.142(b)Storage under appropriate conditions