# FDA Inspection 936300 - Apyx Medical Corporation - July 30, 2015

Source: https://www.keypedia.com/records/fda_inspections/apyx-medical-corporation/6ad519e8-ceb8-4bdc-8e01-7fb43288ef52
Source feed: FDA_Inspections

> FDA Inspection 936300 for Apyx Medical Corporation on July 30, 2015. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 936300
- Company Name: Apyx Medical Corporation
- Inspection Date: 2015-07-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 936300 - 2015-07-30](https://www.keypedia.com/records/fda_inspections/apyx-medical-corporation/1db0f468-bd21-40b7-a14f-c81a454c31f9)
- [FDA Inspection 763375 - 2012-01-18](https://www.keypedia.com/records/fda_inspections/apyx-medical-corporation/7d9bd10c-3a14-4130-a83c-d34f60cb2ea2)
- [FDA Inspection 763375 - 2012-01-18](https://www.keypedia.com/records/fda_inspections/apyx-medical-corporation/161ca880-c276-4aa0-9ded-ea23ae9b64c7)

Company: https://www.keypedia.com/companies/apyx-medical-corporation/bca62a79-266d-4f32-a023-da4c2092a11d

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