FDA Inspection 1293010 — Amgen Inc.

Amgen Inc. — FEI 3003750095

The FDA completed an inspection of Amgen Inc. on November 6, 2025 in Louisville, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 6, 2025
Fiscal Year
2026
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Louisville, KY (United States)