I agree that the letter is petty, and really rando
Post# of 148277
The FDA is like the compliance group at my company. They are beauracrats. They never solve anything. And they see some random thing come across their desk, and make you spend time explaining it - sometimes it's the most minor and irrelevant thing.
As I think Ohm said, we just need to put our heads down, grind, and give them clean, complete data on a trial and move forward. I think that's what we're trying to do now - so again, ironic that they're bringing this up now.