FDA Inspection 805250 - Kevin B Rapeport - October 18, 2012

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Record Details

This FDA Inspection record concerns Kevin B Rapeport, with an inspection on October 18, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: Kevin B Rapeport
Inspection Date: October 18, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · e7be33a0-830c-4bdb-9678-e7be665102d6

Violation Codes1

21 CFR 50.27(a)

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