FDA Inspection 628243 — CVRx, Inc.

CVRx, Inc. — FEI 3007972010

The FDA completed an inspection of CVRx, Inc. on Nov 18, 2009 in Minneapolis, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 18, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Minneapolis, MN (United States)

Additional Details

Sponsor, Contract Research Organization

Citations

IDCFRDescription
292821 CFR 812.40Sponsors' general responsibilities
304321 CFR 812.150(b)(2)Sponsor notification of IRB approval withdrawal