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Plainfield Precision Achieves ISO 13485:2003 Quality Management Certification for Medical Device Manufacturing
Date:7/26/2012

IRVINE, Calif., July 26, 2012 /PRNewswire/ -- Plainfield Precision, a global leader in medical device manufacturing, announced today that it has earned the International Organization for Standardization's (ISO) 13485:2003 certification for their "plastic injection molding, metal stamping, assembly and manufacturing of medical devices". Plainfield Precision's certified quality management system produces the highest quality products and components for its clients based on the stringent requirements set by ISO 13485:2003. The certification cover's Plainfield Precision's facilities in Plymouth Massachusetts, Sturgeon Bay Wisconsin and the Dominican Republic.

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"This certification is an independent confirmation of our dedication to achievement of the highest-quality production and services that meet the needs of our customers," said Jonathan Soucy, President of Plainfield Precision.

Companies receiving the ISO 13485:2003 certification must demonstrate their ability to provide medical devices and related services that consistently meet customer and regulatory requirements. Plainfield Precision's review was completed by NQA (http://www.nqa-usa.com/), one of the largest and most respected ISO registrants in the world.

"Achieving our ISO13485 certification has validated our processes and controls and has demonstrated our commitment to providing high quality products and services to the medical device industry," states Soucy.  "Having this in place will provide our customers with a high degree of confidence in our already well-established medical device manufacturing expertise."

About Plainfield Precision:

Plainfield Precision is a TS16949, ISO9000, and ISO13485 certified custom manufacturer with facilities in the United States, Mexico, and the Domini
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SOURCE Plainfield Precision
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