# SonoCine Inc. – FDA Inspection, Aug 16, 2019

Source: https://www.keypedia.com/records/fda_inspections/sonocine-inc/1fc7fe82-4bb7-43d7-9498-4b21e878a9c2
Source feed: FDA_Inspections

> FDA inspection 1100095 of SonoCine Inc., August 16, 2019. Classification: Official Action Indicated (OAI). 3 citations under 21 CFR parts 812 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: 1100095
- Company Name: SonoCine Inc.
- Inspection Date: 2019-08-16
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- 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 1024900 - 2017-09-11](https://www.keypedia.com/records/fda_inspections/sonocine-inc/5917b580-99a3-4045-9f19-3e1559b65c29)
- [FDA Inspection 877809 - 2014-05-07](https://www.keypedia.com/records/fda_inspections/sonocine-inc/4df665ad-8a22-4c6d-9822-3fc29cbd5379)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/adaliz-santaliz-cruz/47bd4220-e6cc-4582-a4f5-bd4337f92622)

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