Suretek Medical: FDA warns SureTek on sterilization, QC issues

The FDA issued a warning letter it sent to single use device reprocessor SureTek Medical earlier this month over issues with the company's cleaning and validation processes. The letter was in response to an inspection performed between October and November last year, which SureTek Medical responded to 3 times to address the federal watchdog's concerns [...]The post FDA warns SureTek on sterilization, QC issues appeared first on MassDevice.