FDA Inspection 949605 — Viant Holdings, LLC

Viant Holdings, LLC — FEI 1221485

The FDA completed an inspection of Viant Holdings, LLC on November 12, 2015 in Laconia, NH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 12, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Laconia, NH (United States)