# Iowa Lions Eye Bank, Coralville, IA – FDA Inspections

Source: https://www.keypedia.com/companies/iowa-lions-eye-bank/03e4c27b-d7f7-4c82-9a9a-b1e30d043b4f

> Inspection records and compliance data for Iowa Lions Eye Bank in Coralville, Iowa. 7 FDA inspections on record, last inspected October 26, 2023.

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## Details

- Name: Iowa Lions Eye Bank
- FEI Number: 3001238368
- Address Line 1: 2500 Crosspark Rd Ste W300
- City: Coralville
- State: Iowa
- Zip Code: 52241
- Country Name: United States
- Address: 2500 Crosspark Rd Ste W300, Coralville, Iowa 52241, United States
- Country: United States

## Related Documents

- FDA Inspection 1221768 - Iowa Lions Eye Bank - 2023-10-26 — classification: No Action Indicated (NAI), source: FDA, date: October 26, 2023
- FDA Inspection 1155871 - Iowa Lions Eye Bank - 2021-10-20 — classification: No Action Indicated (NAI), source: FDA, date: October 20, 2021
- FDA Inspection 1155871 - Iowa Lions Eye Bank - 2021-10-20 — classification: No Action Indicated (NAI), source: FDA, date: October 20, 2021
- [FDA Inspection 1155871 - Iowa Lions Eye Bank - 2021-10-20](https://www.keypedia.com/records/fda_inspections/iowa-lions-eye-bank/604b86be-2a6b-45ee-b94d-ed8a5b34ea6b) — classification: No Action Indicated (NAI), source: FDA, date: October 20, 2021
- FDA Inspection 1034386 - Iowa Lions Eye Bank - 2017-11-17 — classification: No Action Indicated (NAI), source: FDA, date: November 17, 2017
- FDA Inspection 1034386 - Iowa Lions Eye Bank - 2017-11-17 — classification: No Action Indicated (NAI), source: FDA, date: November 17, 2017
- FDA Inspection 958043 - Iowa Lions Eye Bank - 2016-02-12 — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2016
- FDA Inspection 868847 - Iowa Lions Eye Bank - 2014-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2014
- FDA Inspection 774774 - Iowa Lions Eye Bank - 2012-03-29 — classification: No Action Indicated (NAI), source: FDA, date: March 29, 2012
- FDA Inspection 639867 - Iowa Lions Eye Bank - 2010-01-22 — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2010

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