@stocksa: I'm not sure that's what he said or suggested - but in that context it seems to me that labelling was the last item the FDA were reviewing before finalizing a final decision: because the prudent thing is to not stop at item 8 or 9 out of 10 because there could also be material feedback on item 10 as well.
I don't agree with your oil salesmen point either: they are operating in unchartered territory, they have to keep things in commercial confidence, they can't let any insider information slip... there have been unfavorable outcomes but unfavorable outcomes does not therefore = sn4k3 0il salesman. MAYBE that's incompetence: I wouldn't necessarily say that, but I think what you are suggesting is out of line.
all IMO and good luck.
Ann: Trading Halt, page-54
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