FDA Inspection 694569 — Medtronic Inc.

Medtronic Inc. — FEI 3008114455

The FDA completed an inspection of Medtronic Inc. on Oct 22, 2010 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 22, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Minneapolis, MN (United States)

Additional Details

Sponsor, Contract Research Organization

Citations

IDCFRDescription
1451721 CFR 812.35(a)(1)No approval for changes requiring prior approval