# Medtronic Sofamor Danek USA, Inc - Inspection Records

Source: https://www.keypedia.com/companies/medtronic-sofamor-danek-usa-inc/1803c0d5-74d1-4e22-9d2a-65ddba605290

> Inspection records and compliance data for Medtronic Sofamor Danek USA, Inc in Memphis, Tennessee. Access full analysis and detailed observations.

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## Details

- Name: Medtronic Sofamor Danek USA, Inc
- FEI Number: 3003120897
- City: Memphis
- State: Tennessee
- Country Name: United States
- Address Line 1: 4340 Swinnea Rd Bldg B
- Zip Code: 38118

## Related Documents

- [FDA Inspection 1251904 - Medtronic Sofamor Danek USA, Inc - 2024-10-08](https://www.keypedia.com/records/fda_inspections/medtronic-sofamor-danek-usa-inc/99db4085-669a-4388-ade3-3c288d481d17) — source: FDA, date: October 8, 2024
- [483 - Medtronic Sofamor Danek USA, Inc - 2022-02-17](https://www.keypedia.com/records/483/medtronic-sofamor-danek-usa-inc/be3dca10-5524-420e-934a-59649fb8bf70) — source: FDA, date: February 17, 2022
- [FDA Inspection 1030805 - Medtronic Sofamor Danek USA, Inc - 2017-10-26](https://www.keypedia.com/records/fda_inspections/medtronic-sofamor-danek-usa-inc/53141f5f-3763-4ab0-b765-74389f32eb2c) — classification: No Action Indicated (NAI), source: FDA, date: October 26, 2017
- [FDA Inspection 1030805 - Medtronic Sofamor Danek USA, Inc - 2017-10-26](https://www.keypedia.com/records/fda_inspections/medtronic-sofamor-danek-usa-inc/a291e243-052d-491c-b74f-502e2db0d04a) — classification: No Action Indicated (NAI), source: FDA, date: October 26, 2017
- [FDA Inspection 840625 - Medtronic Sofamor Danek USA, Inc - 2013-07-15](https://www.keypedia.com/records/fda_inspections/medtronic-sofamor-danek-usa-inc/5144be11-4ce3-42c1-bbc7-1c19ee9cf18d) — classification: No Action Indicated (NAI), source: FDA, date: July 15, 2013
- [FDA Inspection 840625 - Medtronic Sofamor Danek USA, Inc - 2013-07-15](https://www.keypedia.com/records/fda_inspections/medtronic-sofamor-danek-usa-inc/063c199f-5b3e-4056-82fe-4a2f4a1281cc) — classification: No Action Indicated (NAI), source: FDA, date: July 15, 2013
- [FDA Inspection 840625 - Medtronic Sofamor Danek USA, Inc - 2013-07-15](https://www.keypedia.com/records/fda_inspections/medtronic-sofamor-danek-usa-inc/1275661e-9a39-4f80-a9b7-dcd2943249a3) — classification: No Action Indicated (NAI), source: FDA, date: July 15, 2013

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