FDA Warning Letter — Janssen Pharmaceuticals, dba Actelion Pharmaceutical

Case 75124 — FEI 3003498827

The FDA took a Warning Letter action against Janssen Pharmaceuticals, dba Actelion Pharmaceutical on September 14, 2010 (South San Francisco, CA). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Janssen Pharmaceuticals, dba Actelion Pharmaceutical
Date
September 14, 2010
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
South San Francisco, CA (United States)