# Csl Plasma, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/csl-plasma-inc/4a3bf0b5-f77d-4dc5-8381-2852efd7e217

> Inspection records and compliance data for Csl Plasma, Inc. in Minneapolis, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: Csl Plasma, Inc.
- FEI Number: 2177738
- City: Minneapolis
- State: Minnesota
- Country Name: United States
- Address Line 1: 304 E Lake St
- Zip Code: 55408

## Related Documents

- [483 - Csl Plasma, Inc. - 2025-02-26](https://www.keypedia.com/records/483/csl-plasma-inc/ae78cd6f-908d-4a71-8e6d-609c5a62c1d0) — source: FDA, date: February 26, 2025
- [FDA Inspection 1262061 - Csl Plasma, Inc. - 2025-02-26](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/04988184-c18f-4d10-b63d-731b37b375ea) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 26, 2025
- [FDA Inspection 1062734 - Csl Plasma, Inc. - 2018-07-18](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/d929de4d-1ee8-4e11-aadf-4da4ef996a8f) — classification: No Action Indicated (NAI), source: FDA, date: July 18, 2018
- [FDA Inspection 958032 - Csl Plasma, Inc. - 2016-01-08](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/58b86d55-6056-4bc8-a103-e1d8919b622a) — classification: No Action Indicated (NAI), source: FDA, date: January 8, 2016
- [FDA Inspection 889317 - Csl Plasma, Inc. - 2014-07-30](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/9c8f3d62-b6a9-45dd-8946-0716e16b21fa) — classification: No Action Indicated (NAI), source: FDA, date: July 30, 2014
- [FDA Inspection 774819 - Csl Plasma, Inc. - 2012-04-03](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/0d1b7691-b504-408c-bf56-79b541ee3911) — classification: No Action Indicated (NAI), source: FDA, date: April 3, 2012
- [FDA Inspection 643462 - Csl Plasma, Inc. - 2010-01-20](https://www.keypedia.com/records/fda_inspections/csl-plasma-inc/94c82769-d4fb-4763-b9e0-ecc590205d2b) — classification: No Action Indicated (NAI), source: FDA, date: January 20, 2010

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