FDA Inspection 635485 - PAJUNK GMBH MEDIZINTECHNOLOGIE - December 17, 2009

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Record Details

This FDA Inspection record concerns PAJUNK GMBH MEDIZINTECHNOLOGIE, with an inspection on December 17, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: PAJUNK GMBH MEDIZINTECHNOLOGIE
Inspection Date: December 17, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 573f89d4-01f0-4e46-95c0-bd01cbfe7788