# UNOX SPA – FDA Inspection, Dec 7, 2023

Source: https://www.keypedia.com/records/fda_inspections/unox-spa/3c01b383-cffe-473b-829b-478af9edead1
Source feed: FDA_Inspections

> FDA inspection 1224297 of UNOX SPA, December 07, 2023. Classification: Voluntary Action Indicated (VAI). 4 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: 1224297
- Company Name: UNOX SPA
- Inspection Date: 2023-12-07
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1270562 - 2025-05-13](https://www.keypedia.com/records/fda_inspections/unox-spa/5628c05a-1fc9-40e5-b95e-e03d7d8c9854)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/francis-pham/9f96b810-0ce5-430f-a710-ae3e60dce78b)
- [Issuing Officer](https://www.keypedia.com/people/goushi-kubota/b129b5a3-8b10-4940-b5c3-02b36aaba8ba)

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