![Rick Pollack, American Hospital Association CEO and President standing in front of United States flag and the AHA seal.](/sites/default/files/2022-04/AT-Rick-Pollack-Perspective-2022-News-900x400.jpg)
The Food and Drug Administration revoked its emergency use authorization for a SARS-CoV-2 antibody test made by Autobio Diagnostics Co. due to concerns with the accuracy of the test when evaluated at the National Institutes of Health’s Frederick National Laboratory for Cancer Research.