Optimal safety, quality and function improves results
AMS Micromedical maintains required annual registration with the U.S. Food and Drug Administration (FDA). Fulfilling this responsibility provides the FDA with information about our establishment/facilities, the medical devices we produce and the activities we perform on those micromedical devices.
FDA registration allows us to continue everyday production and distribution of safe, reputable micro medical solutions while enhancing our nation’s ability to best respond to public health emergencies. Contact us for additional details.