# FDA Inspection 1214395 - Aeton Medical - August 09, 2023

Source: https://www.keypedia.com/records/fda_inspections/aeton-medical/c2ebcef5-49a5-43a8-b3f0-5fe9aeba8825
Source feed: FDA_Inspections

> FDA Inspection 1214395 for Aeton Medical on August 09, 2023. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1214395
- Company Name: Aeton Medical
- Inspection Date: 2023-08-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1214395 - 2023-08-09](https://www.keypedia.com/records/fda_inspections/aeton-medical/5da9c9fb-d05d-43e3-9631-3a97bd43a388)

Company: https://www.keypedia.com/companies/aeton-medical/4adb1881-1c5b-48d0-82ae-70c192709335

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