FDA Warning Letter — Sanofi-Aventis Deutschland GmbH

Case 161496 — FEI 3003195501

The FDA took a Warning Letter action against Sanofi-Aventis Deutschland GmbH on February 8, 2011 (Frankfurt Am Main, Germany). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Sanofi-Aventis Deutschland GmbH
Date
February 8, 2011
Fiscal Year
2011
Product Type
Drugs
Center
CDER
Location
Frankfurt Am Main (Germany)