FDA Inspection 1229768 — Viant Medical, Inc.

Viant Medical, Inc. — FEI 2244012

The FDA completed an inspection of Viant Medical, Inc. on February 16, 2024 in South Plainfield, NJ. 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 16, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
South Plainfield, NJ (United States)