News Reader
02-20-2009, 01:30 AM
The U.S. Food and Drug Administration announced today that California device manufacturer Cardinal Health 303 Inc., formerly known as Alaris Medical Systems Inc., and three of its top executives have signed an amended consent decree to correct violations of current Good Manufacturing Practice (cGMP) requirements in the company's infusion pumps.
More... (http://www.fda.gov/bbs/topics/NEWS/2009/NEW01960.html)
More... (http://www.fda.gov/bbs/topics/NEWS/2009/NEW01960.html)