FDA inspection

Genzyme Flanders: FDA inspection ending Oct 27, 2011

FDA inspection 752272 · Voluntary Action Indicated (VAI) · Geel

Key facts

Inspection ID 752272
Firm Genzyme Flanders
FEI number 3003623839
Address 153 2nd Ave
City Geel
Country Belgium
Fiscal year 2012
Inspection end date Oct 27, 2011
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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