FDA Inspection 1082461 — Breckenridge Pharmaceutical, Inc

Breckenridge Pharmaceutical, Inc — FEI 3006362554

The FDA completed an inspection of Breckenridge Pharmaceutical, Inc on Jan 29, 2019 in Berlin, CT. 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
Jan 29, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Berlin, CT (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)