# FDA Inspection 1073393 - UnitedHealthcare Hearing - November 30, 2018

Source: https://www.keypedia.com/records/fda_inspections/unitedhealthcare-hearing/2ba7dfb3-e20e-4170-80b1-6acf57a90362
Source feed: FDA_Inspections

> FDA Inspection 1073393 for UnitedHealthcare Hearing on November 30, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1073393
- Company Name: UnitedHealthcare Hearing
- Inspection Date: 2018-11-30
- 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 1073393 - 2018-11-30](https://www.keypedia.com/records/fda_inspections/unitedhealthcare-hearing/ab487ac4-61d7-4776-932c-b1719f66f5dc)
- [FDA Inspection 996276 - 2016-12-07](https://www.keypedia.com/records/fda_inspections/unitedhealthcare-hearing/423bf434-4f86-4433-953b-844f4263e995)
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Company: https://www.keypedia.com/companies/unitedhealthcare-hearing/df6bc81f-ae76-4876-870c-00014e5721e8

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