FDA Inspection 805363 — Abeon Medical Corporation

Abeon Medical Corporation — FEI 3008657512

The FDA completed an inspection of Abeon Medical Corporation on October 30, 2012 in Richfield, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 30, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Richfield, OH (United States)