Home > Newsletters > International Medical Device Regulatory Monitor > U.S. GAO Calls for Device Recall Oversight Reform by FDA
International Medical Device Regulatory Monitor
July 2011 | Vol. 19 No. 7
U.S. GAO Calls for Device Recall Oversight Reform by FDA
The U.S. Food and Drug Administration (FDA) should launch a program to routinely and systematically assess device recall information, and use this program to identify strategies for mitigating health risks presented by defective or unsafe devices, the U.S. Government Accountability Office (GAO) says.
ePublishing :: CMS, Hosting & Web Development | © Copyright by FDAnewsAll rights reserved. Do not duplicate or redistribute in any form.