FDA Inspection 749224 — Via Biomedical

Via Biomedical — FEI 3004152466

The FDA completed an inspection of Via Biomedical on Oct 14, 2011 in Maple Grove, MN. 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
Oct 14, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Maple Grove, MN (United States)