Sponsor content
3 result(s) found, displaying 1 to 3
-
Cancellation or suspensionRegulatory action due to The product is not a medical device therefore the certifications made under section 41FD of the Act at the time of application are incorrect., effective 25/11/2020
-
Face mask market actionProduct defect alert following review of quality, effectiveness and regulatory compliance.
-
Face mask market actionProduct defect alert following review of quality, effectiveness and regulatory compliance.