FDA Inspection
Viant Medical CompanyViant Medical Company – FDA Inspection, Sep 11, 2014
Record Details
This FDA Inspection record concerns Viant Medical Company, with an inspection on September 11, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Viant Medical Company
- Inspection Date
- September 11, 2014
- Product Type
- Devices
View Company Profile
ID · ea5b3e11-79fa-400f-94ca-59b26158f7eb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 894949
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Viant Medical Company
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 22, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 29, 2016 | NAI | 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 1066023 - 2018-08-22
- FDA Inspection 977051 - 2016-06-29
- FDA Inspection 802129 - 2012-09-25
- FDA Inspection 702871 - 2010-12-15
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