FDA Inspection 1132885 — Medtronic, Inc.

Medtronic, Inc. — FEI 3015180993

The FDA completed an inspection of Medtronic, Inc. on October 8, 2020 in Sunnyvale, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 8, 2020
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Sunnyvale, CA (United States)