We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
The FDA issued a Form 483 to Full Range Rehab citing problems with its CAPA procedures, acceptance activities, record-keeping and complaint handling. Read More
Three device manufacturing facilities landed Form 483s from the FDA after inspections turned up numerous problems with their CAPA, complaint, training and MDR procedures. Read More