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 » FDA Warns Aesculap for Reporting, Procedural Failures
FDA Warns Aesculap for Reporting, Procedural Failures
October 10, 2011
The FDA warned German devicemaker Aesculap AG for failing to conduct investigations after receiving multiple consumer complaints.