Medical Device Manufacturer, APEC, Announces ISO 13485:2003 Certification

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APEC, a contract manufacturer for the medical device industry, achieved ISO 13485:2003 certification for implementation of a quality management system at their Baldwin Park, CA manufacturing facility.

This includes delivering the best manufacturability for each component, buying the best possible equipment for processing, and minimizing waste, product and process variability.

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APEC, a contract manufacturer for the medical device industry, has achieved ISO 13485:2003 certification for implementation of a quality management system at their California manufacturing facility and global headquarters, located in Baldwin Park.

The certification specifies requirements for a quality management system in which organizations demonstrate the ability to provide medical devices and related services that consistently meet both customer and regulatory requirements.

"APEC is dedicated to providing exceptional customer value above and beyond industry regulations," said David Padgett, Quality Manager, APEC. "This includes delivering the best manufacturability for each component, buying the best possible equipment for processing, and minimizing waste, product and process variability."

The Baldwin Park plant is a 72,000 sq. ft. state-of-the-art manufacturing facility designed for mid to high volume thermoplastic, silicone (LIM), insert and two-shot molding. APEC manufactures a variety of components for medical device OEM's such as catheters, blood oxygenators, needle-access devices, intravenous components, safety syringes, and much more.

For more information on APEC's services call 626-814-9684 or visit http://www.apecplastics.com.

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Holly Bruning
APEC
949-500-7554
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