FDA Inspection 769005 — Huvepharma, Inc.

Huvepharma, Inc. — FEI 1910641

The FDA completed an inspection of Huvepharma, Inc. on February 21, 2012 in Longmont, CO. 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
February 21, 2012
Fiscal Year
2012
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Longmont, CO (United States)

Citations

IDCFRDescription
218121 CFR 226.1Automated equipment - assurance of proper performance
225121 CFR 226.30Design suitable to facilitate maintenance and operation
237921 CFR 226.40(e)Cleaning to prevent contamination of Type A articles