# FDA Inspection 1260082 - Kaneka Corporation - February 06, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/d513f22c-42b9-4ec1-b890-49ea9384592f
Source feed: FDA_Inspections

> FDA Inspection 1260082 for Kaneka Corporation on February 06, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1260082
- Company Name: Kaneka Corporation
- Inspection Date: 2025-02-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1260082 - 2025-02-06](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/9358167c-d586-4ba9-89ee-781a18a035cb)
- [FDA Inspection 1260082 - 2025-02-06](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/10ea1b07-6b46-4d7b-ab6a-ce55eddd6586)
- [FDA Inspection 1260082 - 2025-02-06](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/42846f66-d733-414d-9522-9d0cf2986aae)
- [FDA Inspection 1012619 - 2017-04-19](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/2226ae11-4576-4879-a80e-65cf4b3fb881)
- [FDA Inspection 1012619 - 2017-04-19](https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/db652a43-7e4f-4a25-9a8c-13d9bfa40c1a)

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

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7