Here’s where the water gets muddy for me and a p
Post# of 36537
NGIO is developing the vaccine. The FDA letter clearly states that they received NGIOs request for written response.
So why is this a GNBT 8K? This should be on NHIO letterhead. It should be an NGIO filing.
If GNBT wants to PR it it should say “GNBT Subsidiary NGIO Receives FDA Response”
This is sloppily worded as a GNBT PR. Why is that?