FDA Inspection 858736 - Anne E. Burke, MD - December 13, 2013

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Record Details

This FDA Inspection record concerns Anne E. Burke, MD, with an inspection on December 13, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Anne E. Burke, MD
Inspection Date: December 13, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 05420418-e317-4b14-9187-497861e1dd9b

Violation Codes1

21 CFR 812.140(a)(2)(i)

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