So like most topics that get raised here this one was covered a couple years ago. It was also solved and found to be a non issue. You can search the board for the terms involved to find the old topics and links to regulations. But just to begin with...
The FDA is the federal DRUG administration. Unless we begin trying medical applications they will have nothing to do with us. The EPA could but it is also not their department.
This would be covered by the USDA and APHIS So to begin with ...
So everyone who is worried should do some reading before they build a case about the FDA giving KBLB and issues.
The regulations will become an issue when we are trying to make silk tendons or bones. The FDA is the only regulator that will be an issue and that wont be for 5-10 years or more
Who said worth more as food? Over and above what we get from the various varieties of silk, it will be worth more. (Silk revenues + food revs) But comparing....you are once again correct. This was done for silk and that will definitely be the company maker. Next fringe subject..... your looking for disagreement way too hard.