ITI's PRECISION-QUALITY SYSTEM
ITI has built a Quality Management System designed to satisfy the most stringent of customer requirements across the medical device industry.
Quality is embedded in our processes from the beginning of the development stage with initial prototyping and carried through to the final manufacturing process design. Our design process culminates in a series of strict validation protocols verifying that a robust, efficient, defect free manufacturing process has been achieved.Â
Zero to single digit PPM rates over the years place ITI Quality in the top 5% of our industry based upon industry bench marking reports.
ITI is able to work with all industries and develop products according to the general standards and protocols of those industries while having the expertise to customize requirements to an individual customer’s needs.
VALIDATION METHODOLOGIES AND PROBLEM SOLVING TOOLS USED
Validation Protocols
PPAP (Production Part Approval Process) for Automotive and other customers
Six Sigma problem solving and lean manufacturing principles
DMAIC problem solving model: define, measure, analyze, improve control
5S program ongoing plant wide
ISO CERTIFICATIONS
Our Registrar Audit reports demonstrate multiple years with zero non-conformances and are available for review during customer visits.Â
ISO 13485:2016
SUPPLIER QUALITY REQUIREMENTS (SQR)
QUALITY POLICY
ITI’s Quality Policy is to provide custom, high precision stamped and molded products to a wide range of industries. We are dedicated to achieving customer satisfaction by continually measuring and improving the effectiveness of our quality management system and its objectives. ITI will meet requirements, be on time, and at a competitive price.
CORPORATE PHILOSOPHY
ITI’s corporate philosophy is that every team member is responsible for the quality of all our products and services.Â