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Quality is a priority for Intronix

We had the privilege of going through our regular re-certification ISO audit, which happens every third year in our yearly ISO auditing cycle. This is a top to bottom audit covering all aspects of our regulatory system. Our quality system is registered to both ISO 9001:2000 and ISO 13485:2003. BSI is our quality systems registrar accredited under the Canadian Medical Devices Conformity Assessment System (CMDCAS). These audits are required to maintain our ISO 9001:2000 and ISO 13485:2003 registrations. We have regular internal ISO, FDA, and CE audits to ensure we are performing according to regulation. This is coupled with our regular annual external ISO audit by BSI. We are pleased to have been recommended for re-registration by our ISO auditors at BSI. We have also been recommended for ISO 9001:2008 registration, as we updated to the latest rendition of ISO 9001. We will be updating our website as soon as we receive our new certificates. We at Intronix Technologies Corporation are committed to delivering fault-free products on time, complying with requirements, continually improving the effectiveness of our Quality Management System and satisfying our customers’ needs.