# South Dakota Lions Eye and Tissue Bank Inc. - Inspection Records

Source: https://www.keypedia.com/companies/south-dakota-lions-eye-and-tissue-bank-inc/1733015b-447b-47dc-8d68-1da379b579c0

> Inspection records and compliance data for South Dakota Lions Eye and Tissue Bank Inc. in Bismarck, North Dakota. Access full analysis and detailed observations.

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## Details

- Name: South Dakota Lions Eye and Tissue Bank Inc.
- FEI Number: 3011394216
- City: Bismarck
- State: North Dakota
- Country Name: United States
- Address Line 1: 1003 E Interstate Ave Ste 3
- Zip Code: 58503

## Related Documents

- [FDA Inspection 1240473 - South Dakota Lions Eye and Tissue Bank Inc. - 2024-05-28](https://www.keypedia.com/records/fda_inspections/south-dakota-lions-eye-and-tissue-bank-inc/e7ff07c5-2850-4c17-96dd-eeacc583f55b) — classification: No Action Indicated (NAI), source: FDA, date: May 28, 2024
- [FDA Inspection 1112552 - South Dakota Lions Eye and Tissue Bank Inc. - 2019-11-21](https://www.keypedia.com/records/fda_inspections/south-dakota-lions-eye-and-tissue-bank-inc/7d3b0ccc-5560-435e-a637-5a2831f4bba3) — classification: No Action Indicated (NAI), source: FDA, date: November 21, 2019
- [FDA Inspection 1112552 - South Dakota Lions Eye and Tissue Bank Inc. - 2019-11-21](https://www.keypedia.com/records/fda_inspections/south-dakota-lions-eye-and-tissue-bank-inc/9a6f260f-4cc8-4b52-9ff5-51253336046f) — classification: No Action Indicated (NAI), source: FDA, date: November 21, 2019
- [FDA Inspection 1046163 - South Dakota Lions Eye and Tissue Bank Inc. - 2018-03-20](https://www.keypedia.com/records/fda_inspections/south-dakota-lions-eye-and-tissue-bank-inc/3f2e1804-d32d-442e-9561-423ce5ec4b35) — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2018
- [FDA Inspection 981367 - South Dakota Lions Eye and Tissue Bank Inc. - 2016-08-04](https://www.keypedia.com/records/fda_inspections/south-dakota-lions-eye-and-tissue-bank-inc/9e93427e-285d-45ad-a6ed-0d9a0e5a9a1e) — classification: No Action Indicated (NAI), source: FDA, date: August 4, 2016

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