FDA inspection

Genzyme Flanders: FDA inspection ending Nov 7, 2025

FDA inspection 1290964 · Voluntary Action Indicated (VAI) · Geel

Key facts

Inspection ID 1290964
Firm Genzyme Flanders
FEI number 3003623839
Address Cipalstraat 8
City Geel
Fiscal year 2026
Inspection end date Nov 7, 2025
Classification Voluntary Action Indicated (VAI)
Project area Blood and Blood Products
Product type Biologics

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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