# Medtronic Sofamor Danek USA Inc, Memphis, TN – FDA Inspections

Source: https://www.keypedia.com/companies/medtronic-sofamor-danek-usa-inc/335e1ae6-cdf4-4132-81da-e8914c45ec7c

> Inspection records and compliance data for Medtronic Sofamor Danek USA Inc in Memphis, Tennessee. 13 FDA inspections on record, 1 Form 483, last inspected February 06, 2026.

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## Details

- Name: Medtronic Sofamor Danek USA Inc
- FEI Number: 1000477302
- Address Line 1: 1800 Pyramid Pl
- City: Memphis
- State: Tennessee
- Zip Code: 38132
- Country Name: United States
- Address: 1800 Pyramid Pl, Memphis, Tennessee 38132, United States
- Country: United States

## Related Documents

- FDA Inspection 1302636 - Medtronic Sofamor Danek USA Inc - 2026-02-06 — source: FDA, date: February 6, 2026
- FDA Inspection 1302636 - Medtronic Sofamor Danek USA Inc - 2026-02-06 — classification: No Action Indicated (NAI), source: FDA, date: February 6, 2026
- [FDA Inspection 1029473 - Medtronic Sofamor Danek USA Inc - 2017-05-03](https://www.keypedia.com/records/fda_inspections/medtronic-sofamor-danek-usa-inc/8a05b2e9-77b6-48d5-a949-5271c40a26ac) — source: FDA, date: May 3, 2017
- FDA Inspection 950920 - Medtronic Sofamor Danek USA Inc - 2015-11-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 3, 2015
- FDA Inspection 946127 - Medtronic Sofamor Danek USA Inc - 2015-10-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 23, 2015
- FDA Inspection 946127 - Medtronic Sofamor Danek USA Inc - 2015-10-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 23, 2015
- FDA Inspection 946127 - Medtronic Sofamor Danek USA Inc - 2015-10-23 — classification: No Action Indicated (NAI), source: FDA, date: October 23, 2015
- FDA Inspection 869386 - Medtronic Sofamor Danek USA Inc - 2014-03-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 11, 2014
- FDA Inspection 845563 - Medtronic Sofamor Danek USA Inc - 2013-07-15 — classification: No Action Indicated (NAI), source: FDA, date: July 15, 2013
- FDA Inspection 790663 - Medtronic Sofamor Danek USA Inc - 2012-06-06 — classification: No Action Indicated (NAI), source: FDA, date: June 6, 2012

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