FDA Warning Letter — Breckenridge Pharmaceutical, Inc.

Case 85605 — FEI 3001829070

The FDA took a Warning Letter action against Breckenridge Pharmaceutical, Inc. on Feb 9, 2010 (Boca Raton, FL). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Breckenridge Pharmaceutical, Inc.
Date
Feb 9, 2010
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
Boca Raton, FL (United States)