This forum was paralysed by this question. Is everyone to scared to answer it since management didn't when I was a shareholder at that time.
investors are invited to send questions prior to the webinar lolLast Q&A my question about FDA approval didn't get answered.Marjan Mikel informed attendees at the NWR virtual conference that he will have FDA approval before the end of this quarter as promised.The very concerning issue is the FDA decision was made 11/03/21 8 days prior and volume increased dramatically. Why a trading halt on the 19th after the presentation ????
510(k) Premarket Notification (fda.gov)
Under Listing Rule 3.1, an entity must disclose all information concerning it that it becomes aware of from any source and of any character, if a reasonable person would expect the information to have a material effect on the price or value of its securities.
https://youtu.be/-sc8um4H584
Ann: ADR: Target's Statement, page-9
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