# Kaneka Corporation - Inspection Records

Source: https://www.globalkeysolutions.net/companies/kaneka-corporation/3f38f4de-3d78-415b-91d6-945a7bee153f

> Inspection records and compliance data for Kaneka Corporation in Settsu, None. Access full analysis and detailed observations.

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## Details

- Name: Kaneka Corporation
- FEI Number: 3002808904
- City: Settsu
- State: None
- Country Name: Japan
- Address Line 1: 5 Chome 1-1, Torikainishi
- Zip Code: None

## Related Documents

- [FDA Inspection 1260082 - Kaneka Corporation - 2025-02-06](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/10ea1b07-6b46-4d7b-ab6a-ce55eddd6586) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 6, 2025
- [FDA Inspection 1260082 - Kaneka Corporation - 2025-02-06](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/9358167c-d586-4ba9-89ee-781a18a035cb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 6, 2025
- [FDA Inspection 1260082 - Kaneka Corporation - 2025-02-06](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/42846f66-d733-414d-9522-9d0cf2986aae) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 6, 2025
- [FDA Inspection 1260082 - Kaneka Corporation - 2025-02-06](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/d513f22c-42b9-4ec1-b890-49ea9384592f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 6, 2025
- [FDA Inspection 1012619 - Kaneka Corporation - 2017-04-19](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/db652a43-7e4f-4a25-9a8c-13d9bfa40c1a) — classification: No Action Indicated (NAI), source: FDA, date: April 19, 2017
- [FDA Inspection 1012619 - Kaneka Corporation - 2017-04-19](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/2226ae11-4576-4879-a80e-65cf4b3fb881) — classification: No Action Indicated (NAI), source: FDA, date: April 19, 2017
- [FDA Inspection 962212 - Kaneka Corporation - 2016-03-03](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/3e1baf07-10f6-4bb6-a71e-dcfbcbd9cf4d) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2016
- [FDA Inspection 962212 - Kaneka Corporation - 2016-03-03](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/dc2061d7-85d1-41c5-b9a9-7b2fd87d839c) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2016
- [FDA Inspection 962212 - Kaneka Corporation - 2016-03-03](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/056a77b0-bffc-4502-ab49-ff0018fe6e59) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2016
- [FDA Inspection 800241 - Kaneka Corporation - 2012-09-13](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/574bec02-420c-4a21-86b2-57d1891cbcb5) — classification: No Action Indicated (NAI), source: FDA, date: September 13, 2012

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