FDA Inspection 1021889 - NuPak Medical, Ltd - April 27, 2017

FDA Inspection 1021889 for NuPak Medical, Ltd on April 27, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1021889 for NuPak Medical, Ltd on April 27, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.198(a)

21 CFR 820.75(a)

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Record Information

Company

NuPak Medical, Ltd

Inspection Date

April 27, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa986fe6-75f2-42f6-8a63-cfe0a513113f

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