FDA Warning Letter — Corden Pharma Chenove

Case 46778 — FEI 3002808295

The FDA took a Warning Letter action against Corden Pharma Chenove on May 6, 2009 (Chenove, France). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Corden Pharma Chenove
Date
May 6, 2009
Fiscal Year
2009
Product Type
Drugs
Center
CDER
Location
Chenove (France)