# Medtronic Inc. - Inspection Records

Source: https://www.keypedia.com/companies/medtronic-inc/41386b1c-ad8d-48e3-ab53-fdfbdcab10aa

> Inspection records and compliance data for Medtronic Inc. in Mounds View, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: Medtronic Inc.
- FEI Number: 2182208
- City: Mounds View
- State: Minnesota
- Country Name: United States
- Address Line 1: 8200 Coral Sea St Ne
- Zip Code: 55112

## Related Documents

- [483 - Medtronic Inc. - 2025-02-10](https://www.keypedia.com/records/483/medtronic-inc/041f6c36-79f6-4504-a6d7-5e8ff9a71dbe) — source: FDA, date: February 10, 2025
- [FDA Inspection 1250873 - Medtronic Inc. - 2025-02-10](https://www.keypedia.com/records/fda_inspections/medtronic-inc/4dd1e10d-915e-4d98-a0b0-64eaf59e9e69) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 10, 2025
- [FDA Inspection 1250873 - Medtronic Inc. - 2025-02-10](https://www.keypedia.com/records/fda_inspections/medtronic-inc/6bd08238-e256-47bf-b018-8c33f17fc60f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 10, 2025
- [FDA Inspection 1250873 - Medtronic Inc. - 2025-02-10](https://www.keypedia.com/records/fda_inspections/medtronic-inc/d6c61a17-6f4a-43a1-bb00-143b7dab1b99) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 10, 2025
- [FDA Inspection 1250873 - Medtronic Inc. - 2025-02-10](https://www.keypedia.com/records/fda_inspections/medtronic-inc/10b0a29a-708c-411e-8f41-df75c2c73a53) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 10, 2025
- [FDA Inspection 1217414 - Medtronic Inc. - 2023-09-01](https://www.keypedia.com/records/fda_inspections/medtronic-inc/6f943200-ba29-4b5c-9d5c-470009a415b4) — classification: No Action Indicated (NAI), source: FDA, date: September 1, 2023
- [FDA Inspection 1118989 - Medtronic Inc. - 2020-02-04](https://www.keypedia.com/records/fda_inspections/medtronic-inc/a33d36d9-b6b1-41bd-b9f4-932707fc0f47) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 4, 2020
- [FDA Inspection 1052017 - Medtronic Inc. - 2018-05-14](https://www.keypedia.com/records/fda_inspections/medtronic-inc/fdca1d91-dbf2-4fae-95b0-2488ae45b8ff) — classification: Official Action Indicated (OAI), source: FDA, date: May 14, 2018
- [FDA Inspection 1029345 - Medtronic Inc. - 2017-08-30](https://www.keypedia.com/records/fda_inspections/medtronic-inc/e0518e3e-6951-494f-9178-443a31b3c32c) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2017
- [FDA Inspection 963396 - Medtronic Inc. - 2016-02-29](https://www.keypedia.com/records/fda_inspections/medtronic-inc/34667b82-bf3a-47e9-a68e-d8d9b99eb31e) — classification: No Action Indicated (NAI), source: FDA, date: February 29, 2016
- [FDA Inspection 881795 - Medtronic Inc. - 2014-06-04](https://www.keypedia.com/records/fda_inspections/medtronic-inc/c1fab3cb-e95c-4b4a-b8e1-4b4b20d24603) — classification: No Action Indicated (NAI), source: FDA, date: June 4, 2014

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