FDA Inspection 1221049 — Imhear Corporation

Imhear Corporation — FEI 3011195544

The FDA completed an inspection of Imhear Corporation on September 15, 2023 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 15, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Aurora, IL (United States)