Why the FDA is targeting Google-backed 23andMe: Unnecessary MRIs …

Why the FDA is targeting Google-backed 23andMe: Unnecessary MRIs …

That's all well and good, but the FDA is contending that 23andMe's method of amassing DNA — its Saliva Collection Kit and Personal Genome Service (PGS) – is a class III medical device under the Federal Food, Drug, and Cosmetic Act. The device has not 

2
Like
Save

Comments

Write a comment

*