# Kedplasma LLC - Inspection Records

Source: https://www.keypedia.com/companies/kedplasma-llc/6dad57f8-99cc-4e82-8269-445fb51cb6a0

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

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## Details

- Name: Kedplasma LLC
- FEI Number: 2177765
- City: Houston
- State: Texas
- Country Name: United States
- Address Line 1: 5202 Aldine Mail Route Rd
- Zip Code: 77039

## Related Documents

- [FDA Inspection 1195344 - Kedplasma LLC - 2022-12-06](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/9dd093a0-e1e6-4ac4-bd89-c8027a34580c) — classification: No Action Indicated (NAI), source: FDA, date: December 6, 2022
- [FDA Inspection 1195344 - Kedplasma LLC - 2022-12-06](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/2f408e45-a51c-43bf-a28a-1b6c4ab1cfdf) — classification: No Action Indicated (NAI), source: FDA, date: December 6, 2022
- [FDA Inspection 1010200 - Kedplasma LLC - 2017-04-18](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/55b4e4d6-2657-4472-aaca-3d059f0dee5b) — classification: No Action Indicated (NAI), source: FDA, date: April 18, 2017
- [FDA Inspection 919561 - Kedplasma LLC - 2015-03-11](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/79271138-f83f-4769-a978-e4e55d58882b) — classification: No Action Indicated (NAI), source: FDA, date: March 11, 2015
- [FDA Inspection 831133 - Kedplasma LLC - 2013-04-25](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/771bbc73-475e-4b00-a934-e7bd4dc56720) — classification: No Action Indicated (NAI), source: FDA, date: April 25, 2013
- [FDA Inspection 742311 - Kedplasma LLC - 2011-08-03](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/6fa259d6-2f6d-4f8a-b711-666b41a1c98c) — classification: No Action Indicated (NAI), source: FDA, date: August 3, 2011
- [FDA Inspection 603357 - Kedplasma LLC - 2009-07-21](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/74c3c6ac-45e8-47a6-bbb2-9151408f7570) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2009

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