FDA Inspection 1070919 - Prollenium Medical Technologies Inc. - November 01, 2018

FDA Inspection 1070919 for Prollenium Medical Technologies Inc. on November 01, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1070919 for Prollenium Medical Technologies Inc. on November 01, 2018. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.40

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Record Information

Company

Prollenium Medical Technologies Inc.

Inspection Date

November 1, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 935ea83c-fb57-4192-be65-12eb3ef41d41

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