# Orfit Industries NV – FDA Inspection, May 17, 2018

Source: https://www.keypedia.com/records/fda_inspections/orfit-industries-nv/3d2593ec-9f88-4310-8ad4-55a818e24f49
Source feed: FDA_Inspections

> FDA inspection 1052280 of Orfit Industries NV, May 17, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1052280
- Company Name: Orfit Industries NV
- Inspection Date: 2018-05-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

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- [FDA Inspection 1190273 - 2022-11-10](https://www.keypedia.com/records/fda_inspections/orfit-industries-nv/a0572816-474c-443d-9234-544801849198)
- FDA Inspection 925777 - 2015-02-19

## Related Officers

- [Company Rep](https://www.keypedia.com/people/yehualashet-a-gessesse/cb732900-358c-4982-a912-e98fa45142fe)

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