# FDA Inspection 1195357 - Sonova USA Inc. - December 20, 2022

Source: https://www.keypedia.com/records/fda_inspections/sonova-usa-inc/205f86dc-ec50-4229-8dbb-b737a0a01d02
Source feed: FDA_Inspections

> FDA Inspection 1195357 for Sonova USA Inc. on December 20, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1195357
- Company Name: Sonova USA Inc.
- Inspection Date: 2022-12-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1195357 - 2022-12-20](https://www.keypedia.com/records/fda_inspections/sonova-usa-inc/c9ad7d3a-68de-47c9-a318-d7d1e67d8c82)
- [FDA Inspection 985549 - 2016-08-02](https://www.keypedia.com/records/fda_inspections/sonova-usa-inc/2f247d45-7c01-49ec-90f2-156f4ec2583e)

Company: https://www.keypedia.com/companies/sonova-usa-inc/bf0025e2-9c78-404f-8283-50082770d102

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