FDA Inspection 1090939 — IntriCon Corporation Grey Fox
The FDA completed an inspection of IntriCon Corporation Grey Fox on May 7, 2019 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
- May 7, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Arden Hills, MN (United States)