FDA Warning Letter — Octapharma AB

Case 179372 — FEI 3005559915

The FDA took a Warning Letter action against Octapharma AB on April 15, 2011 (Stockholm, Sweden). The action was issued by CBER and concerns biologics products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Octapharma AB
Date
April 15, 2011
Fiscal Year
2011
Product Type
Biologics
Center
CBER
Location
Stockholm (Sweden)