FDA Inspection 683586 - Mark A Klaassen, M.D. - September 28, 2010

FDA Inspection 683586 for Mark A Klaassen, M.D. on September 28, 2010. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 683586 for Mark A Klaassen, M.D. on September 28, 2010. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 58.130(e)

21 CFR 812.100

21 CFR 812.110(a)

21 CFR 812.110(b)

21 CFR 812.140(a)(1)

21 CFR 812.140(a)(3)(ii)

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Record Information

Company

Mark A Klaassen, M.D.

Inspection Date

September 28, 2010

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fcd5c301-f0b7-410e-b255-73dd2221d0f5

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