FDA Inspection 849682 - Alexander G Digenis MD - September 05, 2013

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Record Details

This FDA Inspection record concerns Alexander G Digenis MD, with an inspection on September 5, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Alexander G Digenis MD
Inspection Date: September 5, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 772e4709-acb1-49c0-ada8-96e062e7c3f4

Violation Codes1

21 CFR 812.140(a)(3)(i)

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