FDA Inspection 729539 - Steven Gaede, MD - June 07, 2011

FDA Inspection 729539 for Steven Gaede, MD on June 07, 2011. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 729539 for Steven Gaede, MD on June 07, 2011. Classification: Voluntary Action Indicated (VAI).

Violation Codes

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

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Record Information

Company

Steven Gaede, MD

Inspection Date

June 7, 2011

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f7d1857c-7c65-49a4-9ef5-9fca07b8efb4

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