FDA Inspection 702871 — Viant Medical Company

Viant Medical Company — FEI 1419629

The FDA completed an inspection of Viant Medical Company on Dec 15, 2010 in Grand Rapids, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 15, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Grand Rapids, MI (United States)

Citations

IDCFRDescription
383721 CFR 820.25(b)Training records
53721 CFR 820.70(a)Production processes