so I have a friend who works at atrium medical and the executive VP of regulatory a tool named Ken Collins is going around telling everybody that they are going into a consent decree with FDA, he has stated that several product lines will be shut down. lots of internal chatter about the mesh product and the synthetic arteries? apparently this guy talks a lot about matters that he should not be talking about to his subordinates. from what I hear the company is a total shit show since it has been sold to getinge/maquet,
atrium/Maquet/Getinge group consent decree??
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