FDA Inspection
Jolife ABFDA Inspection 886118 - Jolife AB - July 02, 2014
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Record Details
This FDA Inspection record concerns Jolife AB, with an inspection on July 2, 2014, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 5867c079-4df5-49c4-8789-ce7d6bea79ee