FDA inspection

Orfit Industries NV: FDA inspection ending Nov 10, 2022

FDA inspection 1190273 · Voluntary Action Indicated (VAI) · Wijnegem

Key facts

Inspection ID 1190273
Firm Orfit Industries NV
FEI number 1000227792
Address Vosveld 9a
City Wijnegem
Country Belgium
Fiscal year 2023
Inspection end date Nov 10, 2022
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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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