FDA Inspection 1009746 - Promedtek, Inc. - April 06, 2017

FDA Inspection 1009746 for Promedtek, Inc. on April 06, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1009746 for Promedtek, Inc. on April 06, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.30(j)

21 CFR 820.50

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Record Information

Company

Promedtek, Inc.

Inspection Date

April 6, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f7fc024c-46fc-4c1c-a37c-46a9fc9436a5

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