FDA Inspection 1001753 — Widex A/S
The FDA completed an inspection of Widex A/S on January 25, 2017 in Lynge. 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
- January 25, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Lynge (Denmark)