# FDA Inspection 1270562 - UNOX SPA - May 13, 2025

Source: https://www.keypedia.com/records/fda_inspections/unox-spa/4dc3eb9e-5b1c-4fba-9a53-b74448a15c2b
Source feed: FDA_Inspections

> FDA Inspection 1270562 for UNOX SPA on May 13, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1270562
- Company Name: UNOX SPA
- Inspection Date: 2025-05-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1270562 - 2025-05-13](https://www.keypedia.com/records/fda_inspections/unox-spa/5628c05a-1fc9-40e5-b95e-e03d7d8c9854)
- [FDA Inspection 1224297 - 2023-12-07](https://www.keypedia.com/records/fda_inspections/unox-spa/3c01b383-cffe-473b-829b-478af9edead1)

Company: https://www.keypedia.com/companies/unox-spa/8eb16927-72f8-452d-b973-4fa1ac2a6c7b

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