FDA Inspection 809682 - MEDIVATORS - December 17, 2012

FDA Inspection 809682 for MEDIVATORS on December 17, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 809682 for MEDIVATORS on December 17, 2012. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.100(a)

21 CFR 820.198(a)

21 CFR 820.200(a)

21 CFR 820.30(h)

21 CFR 820.90(a)

21 CFR 820.90(b)(2)

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Record Information

Company

MEDIVATORS

Inspection Date

December 17, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fac36efd-4880-4959-adc1-a5c7266719cc

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