FDA Inspection 794180 — Celgene Corporation

Celgene Corporation — FEI 3004991673

The FDA completed an inspection of Celgene Corporation on Jul 30, 2012 in Summit, NJ. 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
Jul 30, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Summit, NJ (United States)

Additional Details

Risk Evaluation and Mitigation Strategies (REMS)

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