# FDA Inspection 590452 - Tinnitus Control, Inc. - June 19, 2009

Source: https://www.keypedia.com/records/fda_inspections/tinnitus-control-inc/9c8c635e-1bc2-472d-bfb4-e5f29247b613
Source feed: FDA_Inspections

> FDA Inspection 590452 for Tinnitus Control, Inc. on June 19, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 590452
- Company Name: Tinnitus Control, Inc.
- Inspection Date: 2009-06-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 590452 - 2009-06-19](https://www.keypedia.com/records/fda_inspections/tinnitus-control-inc/bd55eaf4-230d-45ab-946b-3f0d4a5fba6f)

Company: https://www.keypedia.com/companies/tinnitus-control-inc/9a37774e-04b4-481c-98f2-9dfa48a7b886

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