FDA Inspection 1328236 — Valdepharm

Valdepharm — FEI 3000538143

The FDA completed an inspection of Valdepharm on Dec 13, 2024 in Val-De-Reuil. 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). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 13, 2024
Fiscal Year
2025
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Val-De-Reuil (France)

Additional Details

Mutual Recognition Agreement (MRA)

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