FDA Inspection
Viant Medical, Inc.Viant Medical, Inc. – FDA Inspection, May 9, 2012
Record Details
This FDA Inspection record concerns Viant Medical, Inc., with an inspection on May 9, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Viant Medical, Inc.
- Inspection Date
- May 9, 2012
- Product Type
- Devices
View Company Profile
ID · 0520568d-a53b-4999-8da8-ea207e7737db
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 779891
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.75(a)Lack of or inadequate process validation
- 21 CFR 820.100(b)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Viant Medical, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 16, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 22, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 3, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Viant Medical, Inc.
- FDA Inspection 1229768 - 2024-02-16
- FDA Inspection 1114529 - 2019-11-22
- FDA Inspection 649846 - 2010-03-03
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