FDA Inspection 1059004 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3009194033

The FDA completed an inspection of Sanofi Winthrop Industrie on July 13, 2018 in Lyon. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 13, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lyon (France)