FDA Inspection 1044026 — Viant Medical

Viant Medical — FEI 1000514733

The FDA completed an inspection of Viant Medical on February 20, 2018 in Wheeling, IL. 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
February 20, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Wheeling, IL (United States)