FDA inspection

Pfizer Ireland Pharmaceuticals Unlimited Company: FDA inspection ending Jun 17, 2014

FDA inspection 895020 · Voluntary Action Indicated (VAI) · Dublin 22

Key facts

Inspection ID 895020
Firm Pfizer Ireland Pharmaceuticals Unlimited Company
FEI number 3004145594
Address Grange Castle Business Park South, Baldonnell Road
City Dublin 22
Country Ireland
Fiscal year 2014
Inspection end date Jun 17, 2014
Classification Voluntary Action Indicated (VAI)
Project area Vaccines and Allergenic Products
Product type Biologics

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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