FDA Inspection 1005027 — Celgene Corporation

Celgene Corporation — FEI 3004991673

The FDA completed an inspection of Celgene Corporation on Mar 17, 2017 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
Mar 17, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Summit, NJ (United States)

Additional Details

Sponsor, Contract Research Organization

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