FDA Inspection 841677 — Accuvein Inc

Accuvein Inc — FEI 3007121351

The FDA completed an inspection of Accuvein Inc on July 2, 2013 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
July 2, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Medford, NY (United States)