The FDA sends a warning letter to Endo Health's American Medical Systems subsidiary over procedural violations at the Minnetonka, Minn., plant that makes pelvic mesh products.
Endo Health Solutions (NSDQ:ENDP) said the FDA warned it about procedural violations at a Minnesota plant run by its American Medical Systems subsidiary that makes pelvic mesh products.
from MassDevice - FDA and Medical device business news and jobs for the medical device industry http://ift.tt/1j7KSIt
Cap comentari:
Publica un comentari a l'entrada