# Stephanix – FDA Inspection, Sep 14, 2023

Source: https://www.keypedia.com/records/fda_inspections/stephanix/d93a9f2a-859e-4175-ac12-64b26294b73f
Source feed: FDA_Inspections

> FDA inspection 1218225 of Stephanix, September 14, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1218225
- Company Name: Stephanix
- Inspection Date: 2023-09-14
- 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: 2

## Related Officers

- [Kenya Destin](https://www.keypedia.com/people/kenya-destin/1a367d64-8171-4dfd-bb1f-78d8b96a99f5)

Company: https://www.keypedia.com/companies/stephanix/660c9966-8628-4f1f-80b7-ac8dc39bea01

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