FDA Inspection
Medtronic Inc.Medtronic Inc. – FDA Inspection, Aug 16, 2018
Record Details
This FDA Inspection record concerns Medtronic Inc., with an inspection on August 16, 2018, issued by the Minneapolis District Office, covering medical devices & rad health.
- Company
- Medtronic Inc.
- Inspection Date
- August 16, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 9881dcb6-f964-495f-b5b0-257c8af85b16
Inspection Facts
- Inspection number
- 1157919
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Medtronic Inc.
16| Date | Classification | Office | Project area |
|---|---|---|---|
| February 10, 2025 | VAI | Minneapolis District Office | Compliance: Medical Devices |
| September 1, 2023 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| February 4, 2020 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| May 14, 2018 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 16, 2017 | Not classified | Minneapolis District Office |
Other documents for Medtronic Inc.
- FDA Inspection 1250873 - 2025-02-10
- FDA Inspection 1217414 - 2023-09-01
- FDA Inspection 1118989 - 2020-02-04
- FDA Inspection 1052017 - 2018-05-14
- FDA Inspection 1034329 - 2017-11-16
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