FDA Inspection 1211270 — Intervet Production S.A.

Intervet Production S.A. — FEI 3003244826

The FDA completed an inspection of Intervet Production S.A. on Oct 22, 2020 in Igoville. 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
Oct 22, 2020
Fiscal Year
2021
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Igoville (France)

Additional Details

Mutual Recognition Agreement (MRA)

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