# FDA Inspection 800241 - Kaneka Corporation - September 13, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/kaneka-corporation/f743408b-e8d2-4463-9011-9d3eaab455b3/
Source feed: FDA_Inspections

> FDA Inspection 800241 for Kaneka Corporation on September 13, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 800241
- Company Name: Kaneka Corporation
- Inspection Date: 2012-09-13
- 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