The the question is why did the FDA issue an RTF?

The the question is why did the FDA issue an RTF? It is my understanding that the RO results whether you personally give them credence or not were necessary to the FDA and the truth is it wasn’t the quality of the test that was in question but the lack of administration of it. I am long… Nothing would make me happier than for this not to be the case but then why hasn’t there been a single word from management about exactly what is necessary and why it hasn’t been delivered to the FDA?… All they would have to do is say hey it’s this that and the other. End of story...Instead it’s an unending obfuscation and the delay of timelines… Yes?