FDA Inspection 778745 — Nortech Systems, Inc.

Nortech Systems, Inc. — FEI 2183613

The FDA completed an inspection of Nortech Systems, Inc. on April 25, 2012 in Milaca, 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
April 25, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Milaca, MN (United States)