Medical Device Manufacturer’s Director of Clinical Services Pleads Guilty to Causing the Adulteration of Rectal Pressure Sensor
Date of publication: 16-12-2020
FDA OCI, Denise D’Andrea, guilty plea, medical device, adulteration, director, clinical services, Prometheus, device manufacturer, Pathway CTS 2000, pelvic muscle rehabilitation, single-patient use, re-use, cross-contamination, viral, bacterial, diseases, risk, Roger Beyer, Susan Wright, Źródło: http://www.fda.gov
