FDA Inspection 629492 — Viant Holdings, LLC
The FDA completed an inspection of Viant Holdings, LLC on November 9, 2009 in Laconia, NH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- November 9, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Laconia, NH (United States)