# KEDPLASMA, LLC - Inspection Records

Source: https://www.keypedia.com/companies/kedplasma-llc/a3a93a17-aee3-48f6-b4ad-a18182451d10

> Inspection records and compliance data for KEDPLASMA, LLC in Lubbock, Texas. Access full analysis and detailed observations.

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## Details

- Name: KEDPLASMA, LLC
- FEI Number: 1641503
- City: Lubbock
- State: Texas
- Country Name: United States
- Address Line 1: 2415a Main St
- Zip Code: 79401

## Related Documents

- [FDA Inspection 1199764 - KEDPLASMA, LLC - 2023-03-02](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/b3f622f3-6eaf-4982-b597-afcf5d2c086f) — classification: No Action Indicated (NAI), source: FDA, date: March 2, 2023
- [FDA Inspection 1199764 - KEDPLASMA, LLC - 2023-03-02](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/3b7a06d0-e2f9-456c-81b8-89ef0d40d1f3) — classification: No Action Indicated (NAI), source: FDA, date: March 2, 2023
- [FDA Inspection 1017303 - KEDPLASMA, LLC - 2017-05-17](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/4bc63720-f9e0-4dda-a02c-1d3b5136cea4) — classification: No Action Indicated (NAI), source: FDA, date: May 17, 2017
- [FDA Inspection 908003 - KEDPLASMA, LLC - 2014-12-18](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/9be5d07c-5d1d-4990-b824-3e27eefd78dc) — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2014
- [FDA Inspection 835671 - KEDPLASMA, LLC - 2013-06-13](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/cebaf667-da0a-4cb9-8c43-271632f9b117) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 13, 2013
- [FDA Inspection 716334 - KEDPLASMA, LLC - 2011-03-18](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/79402499-9270-4112-8295-73d243020b10) — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2011
- [FDA Inspection 573983 - KEDPLASMA, LLC - 2009-03-20](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/411d8720-e29b-4fe0-8735-70adea87c1ac) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 20, 2009

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