FDA Inspection 560525 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3002808208

The FDA completed an inspection of Sanofi Winthrop Industrie on Jan 23, 2009 in Carbon Blanc CEDEX. 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
Jan 23, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Carbon Blanc CEDEX (France)

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