FDA Inspection 1132885 — Medtronic, Inc.
The FDA completed an inspection of Medtronic, Inc. on Oct 8, 2020 in Sunnyvale, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Oct 8, 2020
- Fiscal Year
- 2021
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Sunnyvale, CA (United States)