FDA Inspection 1041021 — IntriCon Corp

IntriCon Corp — FEI 3007939342

The FDA completed an inspection of IntriCon Corp on December 19, 2017 in Vadnais Heights, 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
December 19, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Vadnais Heights, MN (United States)