# KEDPlasma LLC - Inspection Records

Source: https://www.keypedia.com/companies/kedplasma-llc/fbf82fe6-6e78-4f89-9b45-81c18d3b6af6

> Inspection records and compliance data for KEDPlasma LLC in Lincoln, Nebraska. Access full analysis and detailed observations.

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## Details

- Name: KEDPlasma LLC
- FEI Number: 1720702
- City: Lincoln
- State: Nebraska
- Country Name: United States
- Address Line 1: 2002 N St
- Zip Code: 68510

## Related Documents

- [FDA Inspection 1283322 - KEDPlasma LLC - 2025-10-10](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/7cc5c0fa-b712-4789-895f-6dc2f966897f) — source: FDA, date: October 10, 2025
- [FDA Inspection 1283322 - KEDPlasma LLC - 2025-10-10](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/777c1b4a-23a3-4ac9-8641-83db6071c881) — classification: No Action Indicated (NAI), source: FDA, date: October 10, 2025
- [FDA Inspection 1153598 - KEDPlasma LLC - 2021-09-16](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/57e82651-28d2-4cc4-85f4-9f380784f21d) — classification: No Action Indicated (NAI), source: FDA, date: September 16, 2021
- [FDA Inspection 1153598 - KEDPlasma LLC - 2021-09-16](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/1bb65065-6472-431c-b691-d666486aa405) — classification: No Action Indicated (NAI), source: FDA, date: September 16, 2021
- [FDA Inspection 1032157 - KEDPlasma LLC - 2017-10-19](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/7ce89128-b909-4af4-8677-0669c4f6453e) — classification: No Action Indicated (NAI), source: FDA, date: October 19, 2017
- [FDA Inspection 955258 - KEDPlasma LLC - 2016-01-08](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/72b0ee15-ddf4-4a41-93ba-8ab79f0c9b88) — classification: No Action Indicated (NAI), source: FDA, date: January 8, 2016
- [FDA Inspection 879571 - KEDPlasma LLC - 2014-05-15](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/7a5b6f6b-fa59-4789-b0ce-3efb72585f00) — classification: No Action Indicated (NAI), source: FDA, date: May 15, 2014
- [FDA Inspection 794613 - KEDPlasma LLC - 2012-08-08](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/e78e46a2-4102-4d31-99ac-475b56ffc5ff) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 8, 2012
- [FDA Inspection 695291 - KEDPlasma LLC - 2010-10-22](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/5c75d191-fe94-46b0-a538-468154c73a4e) — classification: No Action Indicated (NAI), source: FDA, date: October 22, 2010
- [FDA Inspection 680508 - KEDPlasma LLC - 2010-08-20](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/a369e341-2e2e-4476-b4fc-ef6551897021) — classification: No Action Indicated (NAI), source: FDA, date: August 20, 2010

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