FDA Inspection 1275526 — Celgene Corporation

Celgene Corporation — FEI 3004991673

The FDA completed an inspection of Celgene Corporation on July 18, 2025 in Summit, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 18, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Summit, NJ (United States)