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Re: rodman post# 10388

Monday, 10/31/2022 10:09:11 AM

Monday, October 31, 2022 10:09:11 AM

Post# of 14173
Pathetic. The FACT that they hadn’t produced test product prior and lead shareholders to believe approval was “imminent “ or “in the near term” speaks volumes about this management team and their PRs. And now they just try to slide it in as typical procedure. This should have started the second they moved to the USA mid approval process.

This is what I meant by “they needed to complete and submit submit a major amendment “ which of course the typical posters refused to believe.

The Fact that they are still “ continu(ing) to assemble required documentation and test its manufacturing process to complete its FDA application” tells a realistic shareholder just how far away the final submission is.
No rational Management team would have EVER submitted a PMA and expected success without doing these things first !

They simply submitted incomplete work so they could continue to say “all required documentation has been submitted “ over and over again.

BTW! Guess the new window of time this opens once the final submission is submitted.
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