FDA Inspection 936096 — Aponos Medical Corporation

Aponos Medical Corporation — FEI 3009893592

The FDA completed an inspection of Aponos Medical Corporation on July 20, 2015 in Kingston, NH. 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
July 20, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Kingston, NH (United States)