FDA Inspection 1124660 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3003282644

The FDA completed an inspection of Sanofi Winthrop Industrie on October 10, 2019 in Tours. 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
October 10, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tours (France)

Additional Details

Mutual Recognition Agreement (MRA)