FDA WARNING_LETTER - Harlin, Stuart MD - May 21, 2010

FDA WARNING_LETTER for Harlin, Stuart MD on May 21, 2010. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Harlin, Stuart MD on May 21, 2010. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 812

21 CFR 812.150(a)(2)

21 CFR 812.140(a)(3)

21 CFR 50

21 CFR 812.140(d)

21 U.S.C. 321(h)

21 CFR 812.110(b)

21 CFR 812.100

21 CFR 812.119

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Record Information

Company

Harlin, Stuart MD

Inspection Date

May 21, 2010

Product Type

Devices

Office

Center for Devices and Radiological Health

People

ID: e74fed3c-69c4-4978-9b2e-5e2ef5f5af09

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