FDA Inspection 1037171 — Intricon Corp

Intricon Corp — FEI 3003007876

The FDA completed an inspection of Intricon Corp on Dec 11, 2017 in Arden Hills, 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
Dec 11, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Arden Hills, MN (United States)

Additional Details

Postmarket Audit Inspections