# FDA Inspection 1012389 - Unitron Hearing Inc - April 04, 2017

Source: https://www.keypedia.com/records/fda_inspections/unitron-hearing-inc/c6767669-5f4a-4ffa-8d1c-2e4a2d049217
Source feed: FDA_Inspections

> FDA Inspection 1012389 for Unitron Hearing Inc on April 04, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1012389
- Company Name: Unitron Hearing Inc
- Inspection Date: 2017-04-04
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 977966 - 2016-01-12](https://www.keypedia.com/records/fda_inspections/unitron-hearing-inc/ff0d9001-3b96-41f2-8880-1146290ec894)
- [FDA Inspection 632332 - 2009-12-03](https://www.keypedia.com/records/fda_inspections/unitron-hearing-inc/0943c62e-df7f-47c2-bd72-f323e4ce8f07)

Company: https://www.keypedia.com/companies/unitron-hearing-inc/3761381a-1a93-4c4a-972c-84b2d28c622d

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