FDA Inspection 750708 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3002808341

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