www.fdanews.com/articles/141980-meas-483-lists-capa-marketing-deviations
MEAS 483 Lists CAPA, Marketing Deviations
November 25, 2011
MEAS US, a subsidiary of Measurement Specialties based in Dayton, Ohio, failed to submit a premarket notification to the FDA for three medical devices it modified, a Form 483 states.
The GMP Letter
The GMP Letter