FDA Inspection 1066346 — Viant Fremont Inc

Viant Fremont Inc — FEI 3003080271

The FDA completed an inspection of Viant Fremont Inc on Aug 14, 2018 in Fremont, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 14, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Fremont, CA (United States)