FDA Inspection 1251770 — Preceptis Medical Inc

Preceptis Medical Inc — FEI 3010610937

The FDA completed an inspection of Preceptis Medical Inc on December 18, 2024 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
December 18, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Golden Valley, MN (United States)