FDA Warning Letter — Sanofi Pasteur Limited

Case 312558 — FEI 3002888623

The FDA took a Warning Letter action against Sanofi Pasteur Limited on July 12, 2012 (North York, Canada). The action was issued by CBER and concerns biologics products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Sanofi Pasteur Limited
Date
July 12, 2012
Fiscal Year
2012
Product Type
Biologics
Center
CBER
Location
North York (Canada)