FDA Inspection 820749 - Eurogentec - January 28, 2013

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Record Details

This FDA Inspection record concerns Eurogentec, with an inspection on January 28, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Eurogentec
Inspection Date: January 28, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b240cd6b-151a-49bd-894d-d9e70e5bee00