FDA inspection

Allergan Pharmaceuticals Ireland: FDA inspection ending Mar 11, 2004

FDA inspection 317535 · Voluntary Action Indicated (VAI) · Westport

Key facts

Inspection ID 317535
Firm Allergan Pharmaceuticals Ireland
FEI number 3002806285
Address Castlebar Road
City Westport
Fiscal year 2004
Inspection end date Mar 11, 2004
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
  • Yes 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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