FDA Warning Letter — Sanofi Winthrop Industrie

Case 309618 — FEI 3002972083

The FDA took a Warning Letter action against Sanofi Winthrop Industrie on Jul 12, 2012 (Marcy-L'Etoile, France). The action was issued by CBER and concerns biologics products. This facility has 4 recent FDA inspections on record.

Action details

Facility
Sanofi Winthrop Industrie
Date
Jul 12, 2012
Fiscal Year
2012
Product Type
Biologics
Center
CBER
Location
Marcy-L'Etoile (France)

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