FDA Inspection 800241 - Kaneka Corporation - September 13, 2012

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

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Record Summary

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

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Record Information

Company

Kaneka Corporation

Inspection Date

September 13, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f743408b-e8d2-4463-9011-9d3eaab455b3

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