FDA Inspection 1005908 - IVF Hartmann AG - January 31, 2017

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Record Details

This FDA Inspection record concerns IVF Hartmann AG, with an inspection on January 31, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: IVF Hartmann AG
Inspection Date: January 31, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 40fc1cd1-f32d-4dab-a382-18c4c207880d