FDA Inspection 1037715 — Aponos Medical Corporation

Aponos Medical Corporation — FEI 3009893592

The FDA completed an inspection of Aponos Medical Corporation on January 10, 2018 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
January 10, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Kingston, NH (United States)