# UNOX SPA – FDA Inspection, May 13, 2025

Source: https://www.keypedia.com/records/fda_inspections/unox-spa/5628c05a-1fc9-40e5-b95e-e03d7d8c9854
Source feed: FDA_Inspections

> FDA inspection 1270562 of UNOX SPA, May 13, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 1010 and 1030. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act (RCHSA) Authority
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 2

## Related Documents

- [FDA Inspection 1224297 - 2023-12-07](https://www.keypedia.com/records/fda_inspections/unox-spa/3c01b383-cffe-473b-829b-478af9edead1)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/fouad-attioui/640028ab-0cdd-43c8-816f-433f19c7ad3d)
- Issuing Officer

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

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8