FDA Inspection 1012583 - Poiesis Medical, LLC - May 22, 2017

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Record Details

This FDA Inspection record concerns Poiesis Medical, LLC, with an inspection on May 22, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Poiesis Medical, LLC
Inspection Date: May 22, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 8c580e3d-414e-4037-9796-a0ebf524e3ea

Violation Codes5

21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.30(a)21 CFR 820.5021 CFR 820.80(b)

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