Home » FDA Warns Extremity Medical on Unreported Defects and Mis-Branded Ortho Devices
FDA Warns Extremity Medical on Unreported Defects and Mis-Branded Ortho Devices
The FDA filed a formal warning against New Jersey-based orthopedics maker Extremity Medical for failures in device surveillance and malfunction reporting.
Mass Device
Mass Device
Upcoming Events
-
23Apr
-
25Apr
-
07May
-
14May
-
30May