FDA Inspection 958547 - CME America, LLC - February 03, 2016

FDA Inspection 958547 for CME America, LLC on February 03, 2016. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 958547 for CME America, LLC on February 03, 2016. Classification: Official Action Indicated (OAI).

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Record Information

Company

CME America, LLC

Inspection Date

February 3, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd40fa95-539d-4274-b2b4-33179896f51e

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