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FDA Inspection 1026365 — Amgen Technology (Ireland) Unlimited Company

Amgen Technology (Ireland) Unlimited Company — FEI 3002808497

The FDA completed an inspection of Amgen Technology (Ireland) Unlimited Company on September 22, 2017 in Dun Laoghaire. 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 22, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dun Laoghaire (Ireland)

Facility

Other inspections at this facility

  • 1241641 (NAI Thu Jul 25 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1221006 (NAI Wed Sep 13 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1228800 (VAI Fri Jul 28 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1114773 (VAI Fri Oct 26 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1067928 (NAI Thu Sep 20 2018 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources