# Orfit Industries NV - Inspection Records

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

> Inspection records and compliance data for Orfit Industries NV in Wijnegem, None. Access full analysis and detailed observations.

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## Details

- Name: Orfit Industries NV
- FEI Number: 1000227792
- City: Wijnegem
- State: None
- Country Name: Belgium
- Address Line 1: Vosveld 9a
- Zip Code: None

## Related Documents

- [FDA Inspection 1311274 - Orfit Industries NV - 2026-04-02](https://www.keypedia.com/records/fda_inspections/orfit-industries-nv/27b21b64-9ecc-40b3-8257-9a83db9a2f96) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 2, 2026
- [FDA Inspection 1190273 - Orfit Industries NV - 2022-11-10](https://www.keypedia.com/records/fda_inspections/orfit-industries-nv/9d84d00a-c4c9-4bba-8dfc-2125c7d48300) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 10, 2022
- [FDA Inspection 1190273 - Orfit Industries NV - 2022-11-10](https://www.keypedia.com/records/fda_inspections/orfit-industries-nv/a0572816-474c-443d-9234-544801849198) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 10, 2022
- [483 - Orfit Industries NV - 2018-05-17](https://www.keypedia.com/records/483/orfit-industries-nv/0394cba2-3ac9-483f-ba0f-2e2f4ca3a250) — source: FDA, date: May 17, 2018
- [FDA Inspection 1052280 - Orfit Industries NV - 2018-05-17](https://www.keypedia.com/records/fda_inspections/orfit-industries-nv/3d2593ec-9f88-4310-8ad4-55a818e24f49) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 17, 2018
- [FDA Inspection 925777 - Orfit Industries NV - 2015-02-19](https://www.keypedia.com/records/fda_inspections/orfit-industries-nv/6254dec9-29f6-43cc-af78-53772f2d6fcb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 19, 2015
- [FDA Inspection 925777 - Orfit Industries NV - 2015-02-19](https://www.keypedia.com/records/fda_inspections/orfit-industries-nv/1b5e3224-09f2-46ba-b122-61c6467c3e31) — classification: No Action Indicated (NAI), source: FDA, date: February 19, 2015

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