Inteprod’s Consistent Record of Zero Findings

Underscores Medical Contract Manufacturer’s
Commitment to Quality, Reliability, and Excellence

Eagleville, PA, June 18, 2021 – 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 June 2021 for the 9th 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.

Contract Manufacturing Services:

Technology Transfer

Design for Manufacturing

Transfer to Manufacturing

Quality Control & Assurance

Device Master Record

Supply Chain Management

Complete Product Assembly

Final Test & Packaging

Ship to End User

Post-Production Support & Services

Product Refurbishment

We know Quality matters. We make lifesaving and life changing medical and diagnostic devices, and we fully understand the complexities of medical devices and the importance of quality, reliability and excellence in medical manufacturing. Together we can move medical innovation forward and change lives worldwide.

Handheld Device plans
Handheld Medical Device

Our Development Services:

Product Design and Development

Design for Manufacturing

Design for Cost Reduction

Quality Assurance & Compliance

cGMP Compliant Documentation

Product & Process Validation & Verification

Management of Software and Firmware Development

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