FDA Inspection 1211270 — Intervet Production S.A.

Intervet Production S.A. — FEI 3003244826

The FDA completed an inspection of Intervet Production S.A. on October 22, 2020 in Igoville. 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
October 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)