FDA inspection

Amgen Technology (Ireland) Unlimited Company: FDA inspection ending Jul 28, 2023

FDA inspection 1228800 · Voluntary Action Indicated (VAI) · Dun Laoghaire

Key facts

Inspection ID 1228800
Firm Amgen Technology (Ireland) Unlimited Company
FEI number 3002808497
Address Pottery Road
City Dun Laoghaire
Country Ireland
Fiscal year 2023
Inspection end date Jul 28, 2023
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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