FDA Warning Letter — Octapharma USA, Inc.

Case 294798 — FEI 3004146033

The FDA took a Warning Letter action against Octapharma USA, Inc. on May 17, 2012 (Paramus, NJ). The action was issued by CBER and concerns biologics products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Octapharma USA, Inc.
Date
May 17, 2012
Fiscal Year
2012
Product Type
Biologics
Center
CBER
Location
Paramus, NJ (United States)