FDA Inspection 835430 - ORGENTEC Diagnostika Gmbh - May 02, 2013

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Record Details

This FDA Inspection record concerns ORGENTEC Diagnostika Gmbh, with an inspection on May 2, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: ORGENTEC Diagnostika Gmbh
Inspection Date: May 2, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · d0c075bd-21d6-4503-9cec-d22c4c9c515c

Violation Codes2

21 CFR 820.12021 CFR 820.25(b)

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