So now you should be able to answer: How did the FDA get to Barrie, Ontario. Here's how they got there. Having submitted a DMF to the FDA there was no visit needed to go to LABS in Barrie. When a U.S. pharmaceutical company that has to follow Federal Law, including FDA, referenced the LABS DMF in their drug submission this then made the FDA go to Barrie for the site visit and evaluate the facility. The FDA approved the Barrie facility which was driven by a U.S. pharmaceutical company calling out the LABS DMF.
We followed the same type of process in the auto industry in qualifying a new supplier sending out a Supplier Quality Specialist for 3 days onsite visit. They had to address any short comings before becoming qualified as a supplier. The purchase order I would issue to a new supplier was only valid if they could pass qualification. I was a "blended buyer", purchasing and Supplier Quality Specialist and would do the onsite 3 days visit.
The roadmap and fundamental mechanics are the same. Now that LABS is FDA approved, they can now ship volume quantities of product as referenced by their DMF to the U.S. pharma company that called out their DMF.
Be patient, it takes some time for investors to have it sink in and digest it so we are in the digestion period now. When you see volumes surging into the millions of shares per day, you will know the herd mentality of investors has figured it out.
Statistically, it's a pretty tight bell curve because all humans have the same type of brain and same intelligence capability.
So just be patient and let that permeate through out the herd. They'll come running.