# FDA Inspection 1218225 - Stephanix - September 14, 2023

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

> FDA Inspection 1218225 for Stephanix on September 14, 2023. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1218225 - 2023-09-14](https://www.keypedia.com/records/fda_inspections/stephanix/53ab061f-ee50-46e6-9925-8a3e4c98083c)

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