FDA Warning Letter — Bracco Diagnostics, Inc.

Case 210573 — FEI 1000307800

The FDA took a Warning Letter action against Bracco Diagnostics, Inc. on January 31, 2012 (Princeton, 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
Bracco Diagnostics, Inc.
Date
January 31, 2012
Fiscal Year
2012
Product Type
Drugs
Center
CDER
Location
Princeton, NJ (United States)