FDA Inspection 1115960 — Bristol-Myers Squibb Company

Bristol-Myers Squibb Company — FEI 3008455069

The FDA completed an inspection of Bristol-Myers Squibb Company on Jan 10, 2020 in Devens, MA. 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). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 10, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Devens, MA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.