# East Tennessee Lions Eye Bank, Knoxville, TN – FDA Inspections

Source: https://www.keypedia.com/companies/east-tennessee-lions-eye-bank/0d53cb5b-3865-4cb4-afdb-2263bc69e78b

> Inspection records and compliance data for East Tennessee Lions Eye Bank in Knoxville, Tennessee. 7 FDA inspections on record, last inspected November 14, 2025.

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## Details

- Name: East Tennessee Lions Eye Bank
- FEI Number: 3002689373
- Address Line 1: 1924 Alcoa Hwy # U-26
- City: Knoxville
- State: Tennessee
- Zip Code: 37920
- Country Name: United States
- Address: 1924 Alcoa Hwy # U-26, Knoxville, Tennessee 37920, United States
- Country: United States

## Related Documents

- FDA Inspection 1294478 - East Tennessee Lions Eye Bank - 2025-11-14 — source: FDA, date: November 14, 2025
- FDA Inspection 1294478 - East Tennessee Lions Eye Bank - 2025-11-14 — classification: No Action Indicated (NAI), source: FDA, date: November 14, 2025
- FDA Inspection 1181188 - East Tennessee Lions Eye Bank - 2022-09-30 — classification: No Action Indicated (NAI), source: FDA, date: September 30, 2022
- FDA Inspection 1181188 - East Tennessee Lions Eye Bank - 2022-09-30 — classification: No Action Indicated (NAI), source: FDA, date: September 30, 2022
- FDA Inspection 1181188 - East Tennessee Lions Eye Bank - 2022-09-30 — classification: No Action Indicated (NAI), source: FDA, date: September 30, 2022
- FDA Inspection 1107123 - East Tennessee Lions Eye Bank - 2019-08-30 — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2019
- FDA Inspection 980027 - East Tennessee Lions Eye Bank - 2016-07-26 — classification: No Action Indicated (NAI), source: FDA, date: July 26, 2016
- FDA Inspection 857483 - East Tennessee Lions Eye Bank - 2013-11-22 — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2013
- FDA Inspection 722996 - East Tennessee Lions Eye Bank - 2011-05-20 — classification: No Action Indicated (NAI), source: FDA, date: May 20, 2011
- FDA Inspection 543426 - East Tennessee Lions Eye Bank - 2008-10-15 — classification: No Action Indicated (NAI), source: FDA, date: October 15, 2008

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