FDA Inspection 1181600 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 1000610805

The FDA completed an inspection of Sanofi Winthrop Industrie on December 3, 2021 in Maisons Alfort. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 3, 2021
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Maisons Alfort (France)

Additional Details

Mutual Recognition Agreement (MRA)