FDA Inspection 1215040 — BioReliance Corporation

BioReliance Corporation — FEI 1122041

The FDA completed an inspection of BioReliance Corporation on August 4, 2023 in Rockville, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 4, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rockville, MD (United States)