FDA Inspection 1038507 - Medical City Plano IRB - January 24, 2018

FDA Inspection 1038507 for Medical City Plano IRB on January 24, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1038507 for Medical City Plano IRB on January 24, 2018. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 56.108(a)(1)

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Record Information

Company

Medical City Plano IRB

Inspection Date

January 24, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: e350a712-069e-4fc3-a440-87e4638f3ca1

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