# FDA Inspection 1012840 - Nytone Medical Products, Inc. - June 05, 2017

Source: https://www.keypedia.com/records/fda_inspections/nytone-medical-products-inc/c94cca0e-a6c3-449b-af33-adf86e36f022
Source feed: FDA_Inspections

> FDA Inspection 1012840 for Nytone Medical Products, Inc. on June 05, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1012840
- Company Name: Nytone Medical Products, Inc.
- Inspection Date: 2017-06-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 861881 - 2014-01-10](https://www.keypedia.com/records/fda_inspections/nytone-medical-products-inc/a6cccb2b-4890-40dd-9044-f1db9f92349d)
- [FDA Inspection 588881 - 2009-06-05](https://www.keypedia.com/records/fda_inspections/nytone-medical-products-inc/52db38ad-41bb-4602-bd7b-d1050ff28f21)
- [FDA Inspection 588881 - 2009-06-05](https://www.keypedia.com/records/fda_inspections/nytone-medical-products-inc/2df15de3-2733-441b-a30a-e110179957b0)

Company: https://www.keypedia.com/companies/nytone-medical-products-inc/f3ed71d0-a781-4da9-b446-dd0f5777853e

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