FDA Inspection 577532 — Breckenridge Pharmaceutical, Inc.

Breckenridge Pharmaceutical, Inc. — FEI 3001829070

The FDA completed an inspection of Breckenridge Pharmaceutical, Inc. on Apr 22, 2009 in Boca Raton, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 22, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Boca Raton, FL (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)