# CSL Plasma Inc. - Inspection Records

Source: https://www.keypedia.com/companies/csl-plasma-inc/2207eaa4-6a3b-48ee-a530-036df3cb4539

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

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## Details

- Name: CSL Plasma Inc.
- FEI Number: 1047137
- City: Louisville
- State: Kentucky
- Country Name: United States
- Address Line 1: 1407 W Jefferson St Ste 100
- Zip Code: 40203

## Related Documents

- [FDA Inspection 1178991 - CSL Plasma Inc. - 2022-09-02](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/df6e724d-7446-44ff-b89f-5364e5f6bbe2) — classification: No Action Indicated (NAI), source: FDA, date: September 2, 2022
- [FDA Inspection 1178991 - CSL Plasma Inc. - 2022-09-02](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/fa451981-440f-4218-a480-74950b5dabb1) — classification: No Action Indicated (NAI), source: FDA, date: September 2, 2022
- [FDA Inspection 1050614 - CSL Plasma Inc. - 2018-04-20](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/2991e7c5-530d-4916-9d70-8c53a352f0ae) — classification: No Action Indicated (NAI), source: FDA, date: April 20, 2018
- [FDA Inspection 959734 - CSL Plasma Inc. - 2016-02-24](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/52ba57e0-c3ed-4738-bb6b-cf151517a9a5) — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2016
- [FDA Inspection 865179 - CSL Plasma Inc. - 2014-02-06](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/884ed38d-fd1d-498b-bef7-18d68e30b75d) — classification: No Action Indicated (NAI), source: FDA, date: February 6, 2014
- [FDA Inspection 751491 - CSL Plasma Inc. - 2011-10-07](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/93a1a713-e89e-4617-994a-627f64583aac) — classification: No Action Indicated (NAI), source: FDA, date: October 7, 2011
- [FDA Inspection 631724 - CSL Plasma Inc. - 2009-11-12](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/b85aa2da-43af-4736-86eb-7a282e0fa3c1) — classification: No Action Indicated (NAI), source: FDA, date: November 12, 2009

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