FDA Inspection 1192937 — Minnetronix, Inc.

Minnetronix, Inc. — FEI 3000203066

The FDA completed an inspection of Minnetronix, Inc. on December 8, 2022 in Saint Paul, 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 8, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)