FDA Inspection 704230 — Bristol-Myers Squibb Company

Bristol-Myers Squibb Company — FEI 1283703

The FDA completed an inspection of Bristol-Myers Squibb Company on Dec 2, 2010 in Wallingford, 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
Dec 2, 2010
Fiscal Year
2011
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Wallingford, CT (United States)

Additional Details

Sponsor, Contract Research Organization