# Mid-South Transplant Foundation, Cordova, TN – FDA Inspections

Source: https://www.keypedia.com/companies/mid-south-transplant-foundation/322c149a-44d0-447c-9465-6f1f53ef9bbe

> Inspection records and compliance data for Mid-South Transplant Foundation in Cordova, Tennessee. 7 FDA inspections on record, last inspected February 06, 2026.

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## Details

- Name: Mid-South Transplant Foundation
- FEI Number: 3003741970
- Address Line 1: 8001 Centerview Pkwy Ste 302
- City: Cordova
- State: Tennessee
- Zip Code: 38018
- Country Name: United States
- Address: 8001 Centerview Pkwy Ste 302, Cordova, Tennessee 38018, United States
- Country: United States

## Related Documents

- FDA Inspection 1303560 - Mid-South Transplant Foundation - 2026-02-06 — source: FDA, date: February 6, 2026
- FDA Inspection 1303560 - Mid-South Transplant Foundation - 2026-02-06 — classification: No Action Indicated (NAI), source: FDA, date: February 6, 2026
- FDA Inspection 1190311 - Mid-South Transplant Foundation - 2022-10-26 — classification: No Action Indicated (NAI), source: FDA, date: October 26, 2022
- FDA Inspection 1190311 - Mid-South Transplant Foundation - 2022-10-26 — classification: No Action Indicated (NAI), source: FDA, date: October 26, 2022
- FDA Inspection 1190311 - Mid-South Transplant Foundation - 2022-10-26 — classification: No Action Indicated (NAI), source: FDA, date: October 26, 2022
- FDA Inspection 1079953 - Mid-South Transplant Foundation - 2019-02-07 — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2019
- FDA Inspection 1079953 - Mid-South Transplant Foundation - 2019-02-07 — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2019
- FDA Inspection 994535 - Mid-South Transplant Foundation - 2016-11-18 — classification: No Action Indicated (NAI), source: FDA, date: November 18, 2016
- FDA Inspection 903615 - Mid-South Transplant Foundation - 2014-11-13 — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2014
- FDA Inspection 840477 - Mid-South Transplant Foundation - 2013-07-11 — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2013

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