# LANXESS Corporation - Inspection Records

Source: https://www.keypedia.com/companies/lanxess-corporation/d4d93912-8e03-47f0-87e8-1aac96f0a44d

> Inspection records and compliance data for LANXESS Corporation in Kalama, WA. Access full analysis and detailed observations.

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## Details

- Name: LANXESS Corporation
- FEI Number: 3022820
- City: Kalama
- State: WA
- Country Name: United States
- Address Line 1: 1296 Nw 3rd St
- Zip Code: 98625-9701

## Related Documents

- [483 - LANXESS Corporation - 2024-09-12](https://www.keypedia.com/records/483/lanxess-corporation/b77334a0-879e-4892-8aba-a2577f402104) — source: FDA, date: September 12, 2024
- [FDA Inspection 1249142 - LANXESS Corporation - 2024-09-12](https://www.keypedia.com/records/fda_inspections/lanxess-corporation/5864e1f8-ffec-40c3-9967-596db88b0aa7) — source: FDA, date: September 12, 2024
- [FDA Inspection 1249142 - LANXESS Corporation - 2024-09-12](https://www.keypedia.com/records/fda_inspections/lanxess-corporation/6dbe036d-939d-481d-92b7-5eeb98204b3c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 12, 2024
- [483 - LANXESS Corporation - 2024-09-09](https://www.keypedia.com/records/483/lanxess-corporation/e85d9fd7-963d-49be-92cd-f164cf2e9903) — source: FDA, date: September 9, 2024
- [FDA Inspection 1203652 - LANXESS Corporation - 2023-04-14](https://www.keypedia.com/records/fda_inspections/lanxess-corporation/9b83054e-fdd7-4163-bbd4-bf052f5d9b9e) — source: FDA, date: April 14, 2023
- [EIR - LANXESS Corporation - 2016-01-15](https://www.keypedia.com/records/eir/lanxess-corporation/e6a5a75d-0d8b-466d-b798-7ac543fba5d5) — source: FDA, date: January 15, 2016
- [483 - LANXESS Corporation - 2016-01-15](https://www.keypedia.com/records/483/lanxess-corporation/b3ec1f98-f973-461c-8de4-90ab45ad85b6) — source: FDA, date: January 15, 2016
- [FDA Inspection 961641 - LANXESS Corporation - 2016-01-15](https://www.keypedia.com/records/fda_inspections/lanxess-corporation/1ee869f3-9bf9-4e73-907a-50e428024ad8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 15, 2016
- [FDA Inspection 858227 - LANXESS Corporation - 2013-12-05](https://www.keypedia.com/records/fda_inspections/lanxess-corporation/d1dbe404-f523-4331-8511-c03324fd9c21) — classification: No Action Indicated (NAI), source: FDA, date: December 5, 2013
- [EIR - LANXESS Corporation - 2013-08-02](https://www.keypedia.com/records/eir/lanxess-corporation/e5e1aaf1-ed4e-44c7-8fa1-6121b4738582) — source: FDA, date: August 2, 2013
- [FDA Inspection 843254 - LANXESS Corporation - 2013-08-02](https://www.keypedia.com/records/fda_inspections/lanxess-corporation/ae74da48-4dc5-4769-8ad9-75093d952d8b) — classification: No Action Indicated (NAI), source: FDA, date: August 2, 2013
- [EIR - LANXESS Corporation - 2009-12-17](https://www.keypedia.com/records/eir/lanxess-corporation/03133058-e89e-40a7-a731-ac912ea27869) — source: FDA, date: December 17, 2009
- [FDA Inspection 637142 - LANXESS Corporation - 2009-12-17](https://www.keypedia.com/records/fda_inspections/lanxess-corporation/41a5cc4f-45fa-430f-b4be-264c3ec39199) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 17, 2009
- [FDA Inspection 547074 - LANXESS Corporation - 2008-11-06](https://www.keypedia.com/records/fda_inspections/lanxess-corporation/f3d440b2-89df-415b-9698-13e4bf23c5ae) — classification: No Action Indicated (NAI), source: FDA, date: November 6, 2008

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