FDA Inspection 913483 — Prevent Products Inc

Prevent Products Inc — FEI 1000049001

The FDA completed an inspection of Prevent Products Inc on Feb 11, 2015 in Saint Paul, MN. 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
Feb 11, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)