Inteprod LLC, a medical device developer and contract manufacturer, announced today that it has received an ISO 13485 Certificate of Registration issued by KEMA Quality B.V. This certification is a major milestone in Inteprod’s 5 year history and confirms Inteprod’s steadfast commitment to continual improvement, risk management, compliance with statutory and regulatory requirements, and complete customer satisfaction.
ISO 13485 is an internationally recognized standardization system which defines the standards for the design, development, production, and distribution of medical devices. It ensures conformity with specified quality controls in the development of safe and effective medical devices.
According to Inteprod’s President and Founder, Rick T. Smethers, “Inteprod continually strives to be the leader in the contract development and manufacture of medical products. This certification is a tribute to Inteprod’s continued focus on exceeding customer expectations, and validates our commitment to high quality standards.”
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