FDA Inspection 1023161 - Synthes Hagendorf GmbH - August 03, 2017

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Record Details

This FDA Inspection record concerns Synthes Hagendorf GmbH, with an inspection on August 3, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Synthes Hagendorf GmbH
Inspection Date: August 3, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 975b5e1d-aff4-4517-a8ad-92a8b25e8e05