FDA inspection

Genzyme Ireland Limited: FDA inspection ending Feb 27, 2014

FDA inspection 886069 · Voluntary Action Indicated (VAI) · Waterford

Key facts

Inspection ID 886069
Firm Genzyme Ireland Limited
FEI number 3003809840
Address Unit 701, Ida Industrial Par; Old Kilmeaden Road
City Waterford
Fiscal year 2014
Inspection end date Feb 27, 2014
Classification Voluntary Action Indicated (VAI)
Project area New Drug Evaluation
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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