FDA Inspection 676642 - Angiomed GmbH & Co. Medizintechnik KG - March 25, 2010

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Record Details

This FDA Inspection record concerns Angiomed GmbH & Co. Medizintechnik KG, with an inspection on March 25, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Angiomed GmbH & Co. Medizintechnik KG
Inspection Date: March 25, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a10ce3fa-acb2-45ae-80f4-0749463a5115