FDA inspection

Baxter R & D Europe: FDA inspection ending Feb 2, 2023

FDA inspection 1207395 · Voluntary Action Indicated (VAI) · Braine-L'Alleud

Key facts

Inspection ID 1207395
Firm Baxter R & D Europe
FEI number 1000359047
Address Boulevard D'Angleterre 2-4
City Braine-L'Alleud
Country Belgium
Fiscal year 2023
Inspection end date Feb 2, 2023
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
  • 1–9 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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