FDA Inspection 808935 - Medefil Incorporated - December 20, 2012

FDA Inspection 808935 for Medefil Incorporated on December 20, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 808935 for Medefil Incorporated on December 20, 2012. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17(a)(1)

21 CFR 820.50(a)(1)

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Record Information

Company

Medefil Incorporated

Inspection Date

December 20, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 1aa287fb-c0e0-4da0-9584-1ab30dc3e10a

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