FDA Inspection
Viant Medical CompanyViant Medical Company – FDA Inspection, Aug 22, 2018
Record Details
This FDA Inspection record concerns Viant Medical Company, with an inspection on August 22, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 4a95b51a-682b-4199-a4b7-ac0a2568476d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1066023
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Viant Medical Company
4| Date | Classification | Office | Project area |
|---|---|---|---|
| June 29, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 11, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 25, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 15, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Viant Medical Company
- FDA Inspection 977051 - 2016-06-29
- FDA Inspection 894949 - 2014-09-11
- FDA Inspection 802129 - 2012-09-25
- FDA Inspection 702871 - 2010-12-15
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