FDA Inspection 750708 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3002808341

The FDA completed an inspection of Sanofi Winthrop Industrie on Sep 29, 2011 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
Sep 29, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Aramon (France)

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