FDA Inspection 1166867 — Aprios Custom Mfg

Aprios Custom Mfg — FEI 3004612223

The FDA completed an inspection of Aprios Custom Mfg on Mar 30, 2022 in Minneapolis, 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
Mar 30, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Minneapolis, MN (United States)