FDA Inspection 1110943 — Widex A/S

Widex A/S — FEI 3003557127

The FDA completed an inspection of Widex A/S on November 21, 2019 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
November 21, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lynge (Denmark)