FDA Inspection 985549 — Sonova USA Inc.
The FDA completed an inspection of Sonova USA Inc. on Aug 2, 2016 in Aurora, IL. 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
- Aug 2, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Aurora, IL (United States)