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FDA Inspection 1313084 — Viant Holdings, LLC

Viant Holdings, LLC — FEI 1221485

The FDA completed an inspection of Viant Holdings, LLC on March 20, 2026 in Laconia, NH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 20, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Laconia, NH (United States)

Facility

Other inspections at this facility

  • 1087339 (NAI Thu Apr 11 2019 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