FDA Inspection
Sonivate Medical, Inc.Sonivate Medical, Inc. – FDA Inspection, May 17, 2017
Record Details
This FDA Inspection record concerns Sonivate Medical, Inc., with an inspection on May 17, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Cynthia L. Gorveatt (Issuing Officer)
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ID · fb571671-68e5-4c58-af5d-6e7fa68ddd19
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1011992
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Sonivate Medical, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 23, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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