FDA inspection

Quintiles IMS Ireland Limited: FDA inspection ending May 21, 2010

FDA inspection 663189 · Voluntary Action Indicated (VAI) · Dublin 3

Key facts

Inspection ID 663189
Firm Quintiles IMS Ireland Limited
FEI number 3004213842
Address Estruary House Block P7, Eastpoint Business Park; Alfie Byrne Road
City Dublin 3
Country Ireland
Fiscal year 2010
Inspection end date May 21, 2010
Classification Voluntary Action Indicated (VAI)
Project area Bioresearch Monitoring
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
  • 1–9 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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