We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » Anchor Products Gets 483 for Repeat MDR Failures
Anchor Products Gets 483 for Repeat MDR Failures
February 3, 2012
Addison, Ill.-based Anchor Products received a Form 483 with repeat observations on medical device reporting (MDR) procedures and handling of customer complaints.