FDA Inspection 1250873 — Medtronic, Inc.

Medtronic, Inc. — FEI 2182208

The FDA completed an inspection of Medtronic, Inc. on February 10, 2025 in Mounds View, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 10, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Mounds View, MN (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation