Rapid Tests for Coronavirus Raise Concerns Over Accuracy
![confused woman staring at paper](https://staging.thevaccinereaction.org/wp-content/uploads/2020/06/confused.jpg)
On Mar. 27, 2020, the U.S. Food and Drug Administration (FDA) issued Emergency Use Authorization (EUA) to pharmaceutical and medical devices company Abbott Laboratories, Inc. of Abbott Park, Illinois for a rapid diagnostic test for the SARS-CoV-2 virus known as ID NOW.1 2 3 “We know how important it is to get point-of-care tests out […]