FDA Inspection 825235 — Aponos Medical Corporation

Aponos Medical Corporation — FEI 3009893592

The FDA completed an inspection of Aponos Medical Corporation on March 27, 2013 in Kingston, NH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 27, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Kingston, NH (United States)

Citations

IDCFRDescription
311821 CFR 820.75(a)Documentation