FDA Inspection 1063199 - Poiesis Medical, LLC - August 23, 2018

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Record Details

This FDA Inspection record concerns Poiesis Medical, LLC, with an inspection on August 23, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Poiesis Medical, LLC
Inspection Date: August 23, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 83ceb945-6e0a-43e0-9d4a-1bf64ceda36e

Violation Codes5

21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.30(g)21 CFR 820.30(i)21 CFR 820.75(a)

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