FDA Inspection 873415 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3002808000

The FDA completed an inspection of Sanofi Winthrop Industrie on Mar 7, 2014 in Vitry-Sur-Seine. 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
Mar 7, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vitry-Sur-Seine (France)

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