FDA Inspection 1016943 - GAMBRO ROSTOCK GMBH - July 06, 2017

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Record Details

This FDA Inspection record concerns GAMBRO ROSTOCK GMBH, with an inspection on July 6, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: GAMBRO ROSTOCK GMBH
Inspection Date: July 6, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 08e8b7e3-2df5-4f79-b144-7f22bddc7baa

Violation Codes4

21 CFR 803.5621 CFR 820.250(a)21 CFR 820.30(g)21 CFR 820.75(a)

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