FDA Inspection 976711 — Preceptis Medical Inc

Preceptis Medical Inc — FEI 3010610937

The FDA completed an inspection of Preceptis Medical Inc on July 11, 2016 in Golden Valley, MN. 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 11, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Golden Valley, MN (United States)