FDA Inspection 660150 - Advanced OrthoPro, Inc. - April 29, 2010

FDA Inspection 660150 for Advanced OrthoPro, Inc. on April 29, 2010. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 660150 for Advanced OrthoPro, Inc. on April 29, 2010. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.180

21 CFR 820.198(a)

21 CFR 820.198(a)(3)

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Record Information

Company

Advanced OrthoPro, Inc.

Inspection Date

April 29, 2010

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 732a0765-59cc-4f77-8d0e-b61d82300239

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