# Medtronic MiniMed, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/medtronic-minimed-inc/a75f6a75-6d10-41f1-8c92-839535f005bf

> Inspection records and compliance data for Medtronic MiniMed, Inc. in Northridge, California. Access full analysis and detailed observations.

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## Details

- Name: Medtronic MiniMed, Inc.
- FEI Number: 3003166194
- City: Northridge
- State: California
- Country Name: United States
- Address Line 1: 18000 Devonshire St
- Zip Code: 91325

## Related Documents

- [FDA Inspection 1226943 - Medtronic MiniMed, Inc. - 2024-01-03](https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/59552d55-dcd3-4022-9409-66e13ec611b8) — classification: No Action Indicated (NAI), source: FDA, date: January 3, 2024
- [483 - Medtronic MiniMed, Inc. - 2023-03-10](https://www.keypedia.com/records/483/medtronic-minimed-inc/0d88e323-7115-44c8-aec9-95d748e3bc5c) — source: FDA, date: March 10, 2023
- [EIR - Medtronic MiniMed, Inc. - 2023-03-10](https://www.keypedia.com/records/eir/medtronic-minimed-inc/f8c687cd-8b0e-4a31-9cc4-7e5e761196dd) — source: FDA, date: March 10, 2023
- [FDA Inspection 1199488 - Medtronic MiniMed, Inc. - 2023-03-10](https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/4e2af4c5-7d47-43c8-940e-2638872d02d7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 10, 2023
- [FDA Inspection 1199488 - Medtronic MiniMed, Inc. - 2023-03-10](https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/8d4837ff-b122-4e9b-96ed-06ae9c86bb88) — classification: No Action Indicated (NAI), source: FDA, date: March 10, 2023
- [483 - Medtronic MiniMed, Inc. - 2021-07-07](https://www.keypedia.com/records/483/medtronic-minimed-inc/dc5fcb93-52a2-45c9-b80b-62c194974da0) — source: FDA, date: July 7, 2021
- [FDA Inspection 1145642 - Medtronic MiniMed, Inc. - 2021-07-07](https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/d6b25b74-2795-4765-834a-59933f9912cb) — classification: Official Action Indicated (OAI), source: FDA, date: July 7, 2021
- [EIR - Medtronic MiniMed, Inc. - 2019-02-15](https://www.keypedia.com/records/eir/medtronic-minimed-inc/1d750d30-1485-45d4-b6ff-6e19fff6114a) — source: FDA, date: February 15, 2019
- [FDA Inspection 1082648 - Medtronic MiniMed, Inc. - 2019-02-15](https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/011e5729-386d-4d0e-9efd-072ef895123d) — classification: No Action Indicated (NAI), source: FDA, date: February 15, 2019
- [FDA Inspection 1082648 - Medtronic MiniMed, Inc. - 2019-02-15](https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/7b3df477-262c-4d51-9407-c280f6d25a86) — classification: No Action Indicated (NAI), source: FDA, date: February 15, 2019
- [EIR - Medtronic MiniMed, Inc. - 2018-03-14](https://www.keypedia.com/records/eir/medtronic-minimed-inc/79bfab82-c285-493a-9d50-a17c4839c5a0) — source: FDA, date: March 14, 2018
- [483 - Medtronic MiniMed, Inc. - 2018-03-14](https://www.keypedia.com/records/483/medtronic-minimed-inc/bd3416e8-e121-4749-ac24-0cd1c7239a43) — source: FDA, date: March 14, 2018
- [FDA Inspection 1044249 - Medtronic MiniMed, Inc. - 2018-03-14](https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/9c7af4d1-7d6a-4212-81ee-da4c3f29e0fb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 14, 2018
- [FDA Inspection 1044249 - Medtronic MiniMed, Inc. - 2018-03-14](https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/b11f541e-5f03-426f-9ea1-e1d9a1df6740) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 14, 2018
- [FDA Inspection 1044249 - Medtronic MiniMed, Inc. - 2018-03-14](https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/e2c4bcf6-e82f-4769-a2c9-ff6b038ba5c6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 14, 2018
- [EIR - Medtronic MiniMed, Inc. - 2017-08-14](https://www.keypedia.com/records/eir/medtronic-minimed-inc/cfc4fd15-38b1-44df-8f31-12b9c9097221) — source: FDA, date: August 14, 2017
- [FDA Inspection 1022946 - Medtronic MiniMed, Inc. - 2017-08-14](https://www.keypedia.com/records/fda_inspections/medtronic-minimed-inc/31b86cc6-d85f-4e4c-9f98-8387256c73f4) — classification: No Action Indicated (NAI), source: FDA, date: August 14, 2017
- [EIR - Medtronic MiniMed, Inc. - 2017-03-24](https://www.keypedia.com/records/eir/medtronic-minimed-inc/0828b285-94be-4c25-ae52-490883206e39) — source: FDA, date: March 24, 2017
- [EIR - Medtronic MiniMed, Inc. - 2016-07-22](https://www.keypedia.com/records/eir/medtronic-minimed-inc/22d25823-3330-4fe7-9644-5a4d8ccf5fe5) — source: FDA, date: July 22, 2016
- [483 - Medtronic MiniMed, Inc. - 2016-07-22](https://www.keypedia.com/records/483/medtronic-minimed-inc/b0db1635-54f6-453c-b9c1-627c7cfaed1a) — source: FDA, date: July 22, 2016

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