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FDA Inspection 1087339 — Viant Holdings, LLC

Viant Holdings, LLC — FEI 1221485

The FDA completed an inspection of Viant Holdings, LLC on April 11, 2019 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
April 11, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Laconia, NH (United States)

Facility

Other inspections at this facility

  • 1313084 (NAI Fri Mar 20 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 949605 (NAI Thu Nov 12 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 885564 (NAI Tue Jul 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 789983 (NAI Fri May 18 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 629492 (VAI Mon Nov 09 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources