Wednesday, February 02, 2022 8:46:59 AM
Immunopass is as important to society today as it was prior to the black eye that the FDA put on Empowered.
IF there was a legitimate EMERGENCY USE for Immunopass before (which I believe there was), that EMERGENCY USE hasn't changed because Empowered sold 2,100 test kits without the FDA's prior approval to do so.
IF there is a public need for Immunopass (which, again, I believe there is), then the FDA is not going to "cut off it's own nose to spite its own face."
Sanction Empowered in any way you want, but don't make the public suffer because of Empowered's stupidity.
I believe, whatever delays the FDA's Class I Recall will have on the final approval of Immunopass for an EUA, those delays will be (very) short lived.
Please note that my posts are for discussion only. They should NOT BE CONSIDERED AS ADVICE FOR YOUR OWN PERSONAL INVESTMENT CHOICES. ALWAYS do your own DD and feel free to question or validate my posts at anytime.
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