FDA Inspection 782410 — Numedis Inc.

Numedis Inc. — FEI 3008494514

The FDA completed an inspection of Numedis Inc. on May 21, 2012 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
May 21, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Isanti, MN (United States)