Suntron achieves new medical compliance

The compliance adds to Suntron's current holding of the ISO 13485 standard. FDA-Good Manufacturing Practice (cGMP) standards are defined by the FDA 21 CFR Part 820 QSR. This QSR forces manufacturers to implement a quality system for designing, manufacturing, packaging, labeling, storing and delivering medical devices sold within the United States. "Suntron's Phoenix facility's recent cGMP compliance and FDA registration are a great help to our medical device customers," says Tom Anderson, Plant Manager. "They allow us to ship products manufactured at Suntron directly to our OEM customers' required locations."