# FDA Inspection 1012619 - Kaneka Corporation - April 19, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/db652a43-7e4f-4a25-9a8c-13d9bfa40c1a
Source feed: FDA_Inspections

> FDA Inspection 1012619 for Kaneka Corporation on April 19, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1012619
- Company Name: Kaneka Corporation
- Inspection Date: 2017-04-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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