FDA Inspection 894949 — Viant Medical Company

Viant Medical Company — FEI 1419629

The FDA completed an inspection of Viant Medical Company on Sep 11, 2014 in Grand Rapids, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 11, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Grand Rapids, MI (United States)

Citations

IDCFRDescription
323721 CFR 820.72(b)Remedial action