FDA approves first tests to screen for tickborne parasite in whole blood and plasma to protect the U.S. blood supply

U.S. Food and Drug Administration (FDA) logo (PRNewsfoto/FDA)SILVER SPRING, Md., March 6, 2018 /PRNewswire-USNewswire/ -- The U.S. Food and Drug Administration today approved the Imugen Babesia microti Arrayed Fluorescent Immunoassay (AFIA), for the detection of antibodies to Babesia microti (B. microti) in human plasma samples, and the Imugen...