It has been pretty well established that the DVis is a LOW DOSE medical device. The article you referred to is involving HIGH DOSE equipment. The Managers involved were apparently ALLOWING APPROVAL of medical machines with HIGH DOSES to be sold when in fact they were supposed to be low dose.
You are comparing apples to oranges here. The article you refer to has no significance to IMGG's Dominion. If there were any truth to the article the Dominion would have already been approved with minimal review.
You certainly can not make a case that IMGG DVis is being "RUSHED" thru the process and not thoroughly reviewed. You are trying to link an article on FDA RED devices to a situation that is the total antithesis of what the article states.
If some FDA Managers had given quick and cursory approval to IMGG's DVis, then you might have a point. As it is, the article proves the exact opposite of what you are stating.
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