FDA Inspection 1016928 - ROWEMED AG - June 22, 2017

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Record Details

This FDA Inspection record concerns ROWEMED AG, with an inspection on June 22, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: ROWEMED AG
Inspection Date: June 22, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 39551b1c-a467-4da7-b0c7-af83cd3fd992

Violation Codes3

21 CFR 820.5021 CFR 820.70(a)21 CFR 820.75(a)

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