FDA Inspection 995256 — Accuvein Inc

Accuvein Inc — FEI 3007121351

The FDA completed an inspection of Accuvein Inc on December 8, 2016 in Medford, NY. 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
December 8, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Medford, NY (United States)