FDA inspection

ORIGIN MEDICAL DEVICES HUNGARY KFT: FDA inspection ending May 8, 2025

FDA inspection 1272862 · No Action Indicated (NAI) · Vac

Key facts

Inspection ID 1272862
Firm ORIGIN MEDICAL DEVICES HUNGARY KFT
FEI number 3029922922
Address Szent Laszlo Ut 36
City Vac
Country Hungary
Fiscal year 2025
Inspection end date May 8, 2025
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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