Medizone Intl. (fka MZEIQ)

[teq0904]

Greeno there is likely nothing for mgmt to share because the EPA is free at any time to take this any way they feel - meaning EPA doesn't provide a nice roadmap of remaining obstacles to study. You just keep coming up with more test data to counter EPA arguments when they show up from out of the blue, and sometimes it takes a long time to get it all together for a rebuttal which pushes the timelines back.
If they are ever stymied by something it is game over until they redesign a new device that would require a new application for, so they are not at that point - it would require a nr.