FDA Inspection 1043607 — Numedis Inc.

Numedis Inc. — FEI 3008494514

The FDA completed an inspection of Numedis Inc. on Feb 27, 2018 in Isanti, 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 27, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Isanti, MN (United States)