FDA inspection

Genzyme Flanders: FDA inspection ending Aug 30, 2016

FDA inspection 983432 · No Action Indicated (NAI) · Geel

Key facts

Inspection ID 983432
Firm Genzyme Flanders
FEI number 3003623839
Address 153 2nd Ave
City Geel
Country Belgium
Fiscal year 2016
Inspection end date Aug 30, 2016
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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

Browse all FDA inspections