FDA Inspection 800717 - AMS (US) Inc. - September 26, 2012

FDA Inspection 800717 for AMS (US) Inc. on September 26, 2012. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 800717 for AMS (US) Inc. on September 26, 2012. Classification: No Action Indicated (NAI).

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Record Information

Company

AMS (US) Inc.

Inspection Date

September 26, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fe187e4b-d5bb-4732-a7a9-8be8b23274d3

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