FDA Inspection 679423 — Medtronic, Inc.

Medtronic, Inc. — FEI 2182208

The FDA completed an inspection of Medtronic, Inc. on Sep 2, 2010 in Mounds View, 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
Sep 2, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Mounds View, MN (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures