# Kaneka Corporation, Settsu, Japan – FDA Inspections

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

> Inspection records and compliance data for Kaneka Corporation in Settsu. 4 FDA inspections on record, 1 Form 483, last inspected February 06, 2025.

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## Details

- Name: Kaneka Corporation
- FEI Number: 3002808904
- Address Line 1: 5 Chome 1-1, Torikainishi
- City: Settsu
- Country Name: Japan
- Address: 5 Chome 1-1, Torikainishi, Settsu, Japan
- Country: Japan

## Related Documents

- [483 - Kaneka Corporation - 2025-02-06](https://www.keypedia.com/records/483/kaneka-corporation/6ae34bc6-182f-4271-8a8f-d9b3ed77c479) — source: FDA, date: February 6, 2025
- FDA Inspection 1260082 - Kaneka Corporation - 2025-02-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 6, 2025
- [FDA Inspection 1260082 - Kaneka Corporation - 2025-02-06](https://www.keypedia.com/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 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 6, 2025
- FDA Inspection 1260082 - Kaneka Corporation - 2025-02-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 6, 2025
- FDA Inspection 1012619 - Kaneka Corporation - 2017-04-19 — classification: No Action Indicated (NAI), source: FDA, date: April 19, 2017
- [FDA Inspection 1012619 - Kaneka Corporation - 2017-04-19](https://www.keypedia.com/records/fda_inspections/kaneka-corporation/db652a43-7e4f-4a25-9a8c-13d9bfa40c1a) — classification: No Action Indicated (NAI), source: FDA, date: April 19, 2017
- FDA Inspection 962212 - Kaneka Corporation - 2016-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2016
- FDA Inspection 962212 - Kaneka Corporation - 2016-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2016
- FDA Inspection 962212 - Kaneka Corporation - 2016-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2016
- FDA Inspection 800241 - Kaneka Corporation - 2012-09-13 — classification: No Action Indicated (NAI), source: FDA, date: September 13, 2012

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