FDA Inspection 659849 - Jolife AB - March 24, 2010

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Record Details

This FDA Inspection record concerns Jolife AB, with an inspection on March 24, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Jolife AB
Inspection Date: March 24, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4b4c1e7d-5f14-4ae7-bbdc-1e1bec26c86b