FDA Inspection 680729 — Amgen, Incorporated

Amgen, Incorporated — FEI 3002892484

The FDA completed an inspection of Amgen, Incorporated on September 3, 2010 in Longmont, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 3, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Longmont, CO (United States)