# Nytone Medical Products, Inc. – FDA Inspection, Jun 5, 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 of Nytone Medical Products, Inc., June 05, 2017. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## 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

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

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