# FDA Inspection 1001753 - Widex A/S - January 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/widex-as/3e0bef50-25ef-44b9-a331-199a3e37d243
Source feed: FDA_Inspections

> FDA Inspection 1001753 for Widex A/S on January 25, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1001753
- Company Name: Widex A/S
- Inspection Date: 2017-01-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1110943 - 2019-11-21](https://www.keypedia.com/records/fda_inspections/widex-as/54ac7899-5487-4539-9e2a-626d40f45448)
- [FDA Inspection 1110943 - 2019-11-21](https://www.keypedia.com/records/fda_inspections/widex-as/ea79c3d2-a348-46a7-aca1-1302c267a986)

Company: https://www.keypedia.com/companies/widex-as/c4e4932f-abba-4559-9605-3e0fb8950c1e

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7