FDA Inspection 816931 - Cambridge Diagnostic Products, Inc. - January 10, 2013

FDA Inspection 816931 for Cambridge Diagnostic Products, Inc. on January 10, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 816931 for Cambridge Diagnostic Products, Inc. on January 10, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Cambridge Diagnostic Products, Inc.

Inspection Date

January 10, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc4e7e67-eefd-4d9b-b471-146f5d30784a

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