FDA Inspection
Viant AS&O Holdings, LLCViant AS&O Holdings, LLC – FDA Inspection, Dec 9, 2021
Record Details
This FDA Inspection record concerns Viant AS&O Holdings, LLC, with an inspection on December 9, 2021, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Viant AS&O Holdings, LLC
- Inspection Date
- December 9, 2021
- Product Type
- Devices
View Company Profile
ID · 4734a5a6-6ea8-4c11-8198-215d7d00bcaa
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1159980
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
- 21 CFR 820.184DHR content
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Viant AS&O Holdings, LLC
3| Date | Classification | Office | Project area |
|---|---|---|---|
| October 28, 2024 | NAI | New England District Office | Postmarket Assurance: Medical Devices |
| December 8, 2011 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| August 18, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Viant AS&O Holdings, LLC
- FDA Inspection 1252737 - 2024-10-28
- FDA Inspection 756561 - 2011-12-08
- FDA Inspection 676324 - 2010-08-18
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