# FDA Inspection 962212 - Kaneka Corporation - March 03, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/dc2061d7-85d1-41c5-b9a9-7b2fd87d839c
Source feed: FDA_Inspections

> FDA Inspection 962212 for Kaneka Corporation on March 03, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 962212
- Company Name: Kaneka Corporation
- Inspection Date: 2016-03-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: 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/d513f22c-42b9-4ec1-b890-49ea9384592f)
- [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)

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