FDA Inspection 791521 - Mark Hoyer, M.D. - July 16, 2012

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Record Details

This FDA Inspection record concerns Mark Hoyer, M.D., with an inspection on July 16, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: Mark Hoyer, M.D.
Inspection Date: July 16, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 5b4bd918-3af1-41ee-975d-d1a683b0ace9

Violation Codes5

21 CFR 812.110(b)21 CFR 812.140(a)(1)21 CFR 812.140(a)(2)(i)21 CFR 812.140(d)21 CFR 812.150(a)(1)

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