FDA Inspection 838673 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3002972083

The FDA completed an inspection of Sanofi Winthrop Industrie on Jun 21, 2013 in Marcy-L'Etoile. 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: Biologics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 21, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Marcy-L'Etoile (France)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.