FDA Inspection 1118089 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3002808341

The FDA completed an inspection of Sanofi Winthrop Industrie on Mar 29, 2019 in Aramon. 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: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 29, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Aramon (France)

Additional details

Mutual Recognition Agreement (MRA)

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