# Orfit Industries NV – FDA Inspection, Nov 10, 2022

Source: https://www.keypedia.com/records/fda_inspections/orfit-industries-nv/a0572816-474c-443d-9234-544801849198
Source feed: FDA_Inspections

> FDA inspection 1190273 of Orfit Industries NV, November 10, 2022. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1190273
- Company Name: Orfit Industries NV
- Inspection Date: 2022-11-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1311274 - 2026-04-02](https://www.keypedia.com/records/fda_inspections/orfit-industries-nv/27b21b64-9ecc-40b3-8257-9a83db9a2f96)
- [FDA Inspection 1052280 - 2018-05-17](https://www.keypedia.com/records/fda_inspections/orfit-industries-nv/3d2593ec-9f88-4310-8ad4-55a818e24f49)
- FDA Inspection 925777 - 2015-02-19

Company: https://www.keypedia.com/companies/orfit-industries-nv/3ec06979-5df4-4961-97b7-eccebb8ed53e

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7