FDA Inspection 943216 — Imhear Corporation
The FDA completed an inspection of Imhear Corporation on September 24, 2015 in Aurora, IL. 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
- September 24, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Aurora, IL (United States)