FDA Inspection 785234 — CVRx, Inc.

CVRx, Inc. — FEI 3007972010

The FDA completed an inspection of CVRx, Inc. on May 31, 2012 in Minneapolis, 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
May 31, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Minneapolis, MN (United States)