Arrayit Corporation (ARYC)

[Alyssa]

You are wrong! The FDA did NOT reject the test. The 85.7% sensitivity and 88.1% specificity did not at the time qualify for a EUA, so the FDA converted it to a “Pre--Emergency Use Authorization.” Arrayit and its Covid 19 test is STILL on the FDA’s list as of 6/15/20...yesterday. The FDA did not tell Arrayit to stop offering their test. According to Mark last week, they are continuing to work with the FDA.

If these aren’t signs that ARYC’s test is still in the running, then I don’t know what is.