FDA inspection

Genzyme Flanders: FDA inspection ending Mar 23, 2018

FDA inspection 1049261 · No Action Indicated (NAI) · Geel

Key facts

Inspection ID 1049261
Firm Genzyme Flanders
FEI number 3003623839
Address Cipalstraat 8
City Geel
Country Belgium
Fiscal year 2018
Inspection end date Mar 23, 2018
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

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