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FDA Inspection 619092 — Huvepharma Inc.

Huvepharma Inc. — FEI 1940172

The FDA completed an inspection of Huvepharma Inc. on September 10, 2009 in Saint Louis, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 10, 2009
Fiscal Year
2009
Product Type
Veterinary
Project Area
Pre-Approval Eval. of Animal Drugs and Food Additives
Location
Saint Louis, MO (United States)

Facility

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Recent compliance actions

FDA data resources