FDA Inspection 841677 — Accuvein Inc

Accuvein Inc — FEI 3007121351

The FDA completed an inspection of Accuvein Inc on Jul 2, 2013 in Medford, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 2, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Medford, NY (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.