FDA Inspection 650751 — Nortech Systems, Inc.

Nortech Systems, Inc. — FEI 2183613

The FDA completed an inspection of Nortech Systems, Inc. on March 4, 2010 in Milaca, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 4, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Milaca, MN (United States)

Citations

IDCFRDescription
310221 CFR 820.30(h)Design transfer - Lack of or inadequate procedures