Inteprod’s Consistent Record of Zero Findings & ISO 13485:2016 re-certification

Eagleville, PA, July, 16 2025 – Inteprod LLC, a medical contract manufacturer, announced today that the company once again successfully achieved ISO 13485:2016 re-certification audit with zero findings.

Inteprod achieved ISO 13485:2016 re-certification audit in August 2024 for the 11th year in a row resulted in zero findings, and further confirmed Inteprod’s unwavering commitment to quality, reliability, and excellence in medical product manufacturing.

ISO 13485:2016 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 and manufacture of safe and effective medical devices.

“Achieving and maintaining a consistent record of zero findings is no small feat”, stated Suzanne Smethers, Inteprod’s President. “The auditor’s objective is to find nonconformance(s). Inteprod’s record of multiple audits with zero findings reflects our team’s experience, diligence, and dedication to quality and excellence. At Inteprod, we know the medical products we produce for our clients save and enhance lives around the world; and, for us, Quality matters – a lot!”

The scope of Inteprod’s recertification and move verification include the contract design, development, and manufacture of electromechanical medical devices, medical diagnostics, and consumables.