FDA Inspection 763375 — Apyx Medical Corporation

Apyx Medical Corporation — FEI 3007593903

The FDA completed an inspection of Apyx Medical Corporation on Jan 18, 2012 in Clearwater, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 18, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Clearwater, FL (United States)

Citations

IDCFRDescription
337521 CFR 820.198(e)Records of complaint investigation
369621 CFR 820.100(b)Documentation