# SonoCine Inc. – FDA Inspection, Sep 11, 2017

Source: https://www.keypedia.com/records/fda_inspections/sonocine-inc/5917b580-99a3-4045-9f19-3e1559b65c29
Source feed: FDA_Inspections

> FDA inspection 1024900 of SonoCine Inc., September 11, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024900
- Company Name: SonoCine Inc.
- Inspection Date: 2017-09-11
- 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: 3

## Related Documents

- [FDA Inspection 1100095 - 2019-08-16](https://www.keypedia.com/records/fda_inspections/sonocine-inc/1fc7fe82-4bb7-43d7-9498-4b21e878a9c2)
- [FDA Inspection 877809 - 2014-05-07](https://www.keypedia.com/records/fda_inspections/sonocine-inc/4df665ad-8a22-4c6d-9822-3fc29cbd5379)

## Related Officers

- [Investigator](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)

Company: https://www.keypedia.com/companies/sonocine-inc/2b65ee06-f655-4916-8561-88c9d6a698f7

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