“If it isn’t documented, it didn’t happen” is one of the FDA’s best-known unwritten rules. As the agency’s resources are already stretched thin, the medical device industry is being held to an
ever-higher standard of data collection.
With accurate and comprehensive computer-aided inspection (CAI) you can satisfy regulators by recording and documenting every surface data point and every extracted dimension for future reference — while cutting iterations, months, and millions of dollars from the process development schedule. The same can hardly be said for fixed gauges or optical-comparator overlays!
Visit www.level3inspection.com or call us today to learn more!
