FDA Warning Letter — CorePharma, LLC

Case 96446 — FEI 3002535019

The FDA took a Warning Letter action against CorePharma, LLC on June 21, 2010 (Middlesex, NJ). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
CorePharma, LLC
Date
June 21, 2010
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
Middlesex, NJ (United States)