# Sonivate Medical, Inc. – FDA Inspection, May 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/sonivate-medical-inc/fb571671-68e5-4c58-af5d-6e7fa68ddd19
Source feed: FDA_Inspections

> FDA inspection 1011992 of Sonivate Medical, Inc., May 17, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1011992
- Company Name: Sonivate Medical, Inc.
- Inspection Date: 2017-05-17
- 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: 0

## Related Documents

- [FDA Inspection 863056 - 2014-01-23](https://www.keypedia.com/records/fda_inspections/sonivate-medical-inc/8f70a409-1696-4bb7-bc87-02c71875064f)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/sonivate-medical-inc/5fb88415-b4d8-45f2-acef-a86011eea5ce

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