# CSL Plasma Inc. - Inspection Records

Source: https://www.keypedia.com/companies/csl-plasma-inc/cff6fbdc-b868-4352-adc3-3cd568d453e9

> Inspection records and compliance data for CSL Plasma Inc. in Lawrence, Kansas. Access full analysis and detailed observations.

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## Details

- Name: CSL Plasma Inc.
- FEI Number: 1931585
- City: Lawrence
- State: Kansas
- Country Name: United States
- Address Line 1: 816 W 24th St Ste B
- Zip Code: 66046

## Related Documents

- [FDA Inspection 1192853 - CSL Plasma Inc. - 2022-12-01](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/b4122534-03eb-4881-b286-b67c68c08745) — classification: No Action Indicated (NAI), source: FDA, date: December 1, 2022
- [FDA Inspection 1192853 - CSL Plasma Inc. - 2022-12-01](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/2a878098-2f70-4f6c-9244-6c3f21cb3a16) — classification: No Action Indicated (NAI), source: FDA, date: December 1, 2022
- [FDA Inspection 1032405 - CSL Plasma Inc. - 2017-11-14](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/ecbb284c-4b6a-454f-90ac-bbe8a410a0d5) — classification: No Action Indicated (NAI), source: FDA, date: November 14, 2017
- [FDA Inspection 925402 - CSL Plasma Inc. - 2015-04-17](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/56707f47-ac7c-45f6-b9f1-4a703404cf66) — classification: No Action Indicated (NAI), source: FDA, date: April 17, 2015
- [FDA Inspection 861630 - CSL Plasma Inc. - 2014-01-09](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/8ccd51cd-ceb5-4353-96f5-38f42944d477) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 9, 2014
- [FDA Inspection 770772 - CSL Plasma Inc. - 2012-02-03](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/73187ea7-78fa-40c0-8b4c-65ac9382d9e1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 3, 2012
- [FDA Inspection 671360 - CSL Plasma Inc. - 2010-06-23](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/1656665c-ae6a-4dbb-9a83-fe6e4646832e) — classification: No Action Indicated (NAI), source: FDA, date: June 23, 2010

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