FDA Inspection 1083235 — Bristol-Myers Squibb Company

Bristol-Myers Squibb Company — FEI 3002708128

The FDA completed an inspection of Bristol-Myers Squibb Company on Mar 7, 2019 in Princeton, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 7, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Princeton, NJ (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)

Citations

IDCFRDescription
683521 CFR 314.80(d)Failure to submit scientific article