# Sonablate Corp. – FDA Inspection, Nov 29, 2017

Source: https://www.keypedia.com/records/fda_inspections/sonablate-corp/e85e4ea9-87bd-4627-b6a1-f1ce6098b935
Source feed: FDA_Inspections

> FDA inspection 1032390 of Sonablate Corp., November 29, 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: 1032390
- Company Name: Sonablate Corp.
- Inspection Date: 2017-11-29
- 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 1176147 - 2022-08-02](https://www.keypedia.com/records/fda_inspections/sonablate-corp/25b6b6fb-9f5a-4d04-8468-472053462bc8)
- FDA Inspection 874159 - 2014-03-26

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/gamal-a-norton/6b52c9e6-d579-4994-81ee-e734eb1f0a67)

Company: https://www.keypedia.com/companies/sonablate-corp/a8e942d3-47f4-4e7b-a995-ed7cc79635a7

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