FDA inspection

Eurofins Bactimm B.V.: FDA inspection ending Jul 6, 2023

FDA inspection 1253685 · Voluntary Action Indicated (VAI) · Nijmegen

Key facts

Inspection ID 1253685
Firm Eurofins Bactimm B.V.
FEI number 3002566308
Address Middenkampweg 19
City Nijmegen
Country Netherlands
Fiscal year 2023
Inspection end date Jul 6, 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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