# CSL Behring GmbH - Inspection Records

Source: https://www.globalkeysolutions.net/companies/csl-behring-gmbh/21a38e53-2e5d-4c9e-a287-79597f091cc6

> Inspection records and compliance data for CSL Behring GmbH in Hesse, 35041. Access full analysis and detailed observations.

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## Details

- Name: CSL Behring GmbH
- FEI Number: 3003098680
- City: Hesse
- State: 35041
- Country Name: Germany
- Address Line 1: Marburg
- Zip Code: Germany

## Related Documents

- [WARNING_LETTER - CSL Behring GmbH - Unknown Date](https://www.globalkeysolutions.net/records/warning_letter/csl-behring-gmbh/da7396b2-3718-41b6-8359-b772ae018755) — source: FDA, date: Invalid Date
- [FDA Inspection 1298394 - CSL Behring GmbH - 2026-02-18](https://www.globalkeysolutions.net/records/fda_inspections/csl-behring-gmbh/f8a87b5f-9dec-4c70-bad4-9b3c1f7e7c44) — source: FDA, date: February 18, 2026
- [FDA Inspection 1298394 - CSL Behring GmbH - 2026-02-18](https://www.globalkeysolutions.net/records/fda_inspections/csl-behring-gmbh/914f52dd-c8d2-40d7-a90c-34c9fa7ec604) — source: FDA, date: February 18, 2026
- [FDA Inspection 1298394 - CSL Behring GmbH - 2026-02-18](https://www.globalkeysolutions.net/records/fda_inspections/csl-behring-gmbh/6f5be157-f53f-42b2-97ad-463453dd2735) — source: FDA, date: February 18, 2026
- [483 - CSL Behring GmbH - 2024-04-30](https://www.globalkeysolutions.net/records/483/csl-behring-gmbh/0bb3ff8a-a102-40f7-b84a-b9e4f0208242) — source: FDA, date: April 30, 2024
- [483 - CSL Behring GmbH - 2024-04-18](https://www.globalkeysolutions.net/records/483/csl-behring-gmbh/5e869e2f-39c4-427a-a730-ed3f66a5957b) — source: FDA, date: April 18, 2024
- [483 - CSL Behring GmbH - 2024-04-18](https://www.globalkeysolutions.net/records/483/csl-behring-gmbh/ca2ced1c-5c71-4740-af7b-1686b0a70fc5) — source: FDA, date: April 18, 2024
- [483 - CSL Behring GmbH - 2022-03-04](https://www.globalkeysolutions.net/records/483/csl-behring-gmbh/45772e3f-dea9-45ad-b478-23cd419f7dbe) — source: FDA, date: March 4, 2022
- [FDA Inspection 1166653 - CSL Behring GmbH - 2022-03-04](https://www.globalkeysolutions.net/records/fda_inspections/csl-behring-gmbh/6e2428af-c959-491d-8208-28bca0e31548) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 4, 2022
- [FDA Inspection 1166653 - CSL Behring GmbH - 2022-03-04](https://www.globalkeysolutions.net/records/fda_inspections/csl-behring-gmbh/7271d85f-0630-4cc2-9469-cd86ba2483e9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 4, 2022
- [483 - CSL Behring GmbH - 2018-05-17](https://www.globalkeysolutions.net/records/483/csl-behring-gmbh/ff548397-dc14-4b14-8664-389d7c724d1c) — source: FDA, date: May 17, 2018
- [483 - CSL Behring GmbH - 2018-05-17](https://www.globalkeysolutions.net/records/483/csl-behring-gmbh/e8c1c8f8-2bbb-4021-a093-576c7317ffce) — source: FDA, date: May 17, 2018
- [FDA Inspection 1007037 - CSL Behring GmbH - 2016-05-17](https://www.globalkeysolutions.net/records/fda_inspections/csl-behring-gmbh/8fb67719-f1e3-411a-874f-47052898af3f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 17, 2016
- [FDA Inspection 786201 - CSL Behring GmbH - 2012-01-27](https://www.globalkeysolutions.net/records/fda_inspections/csl-behring-gmbh/e5a09e43-1077-4362-a141-c2cb98093da5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 27, 2012
- [FDA Inspection 655495 - CSL Behring GmbH - 2010-03-18](https://www.globalkeysolutions.net/records/fda_inspections/csl-behring-gmbh/17189a3d-f5f5-4edb-a812-38dc37321a23) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 18, 2010
- [FDA Inspection 655495 - CSL Behring GmbH - 2010-03-18](https://www.globalkeysolutions.net/records/fda_inspections/csl-behring-gmbh/4c89b32a-6210-45ff-9fd2-196f3a72234f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 18, 2010
- [FDA Inspection 655495 - CSL Behring GmbH - 2010-03-18](https://www.globalkeysolutions.net/records/fda_inspections/csl-behring-gmbh/becad389-d5d2-44b8-b06e-5033243e019b) — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2010

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