Axim Biotechnologies Inc (AXIM)

[TexasMarvL]

What this release fails to mention is the FDA Approved 510K test is a Class II test and has to be performed at a CLIA approved lab.

Until AXIM receives a waiver from the FDA all of these tests have to be sent to an approved lab.

Or the eye doctors office has to become CLIA compliant.

I believe page 42 of the 10-Q is a more honest representation of the truth.