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FDA Compliance

Accellent Receives Registration to ISO 13485

Published: Tuesday, August 23, 2005 - 22:00

A recent companywide registration to ISO 13485 marked Accellent Inc.’s commitment to continuous improvement and zero defects, company officials recently reported.The standard applies specifically to the medical device industry and requires continuous improvement and reliable product quality.

“This certification demonstrates our ongoing commitment to providing the highest-quality products and services to our medical device clients,” says Ron Sparks, Accellent president and CEO. “Quality is of the highest importance to our customers and every Accellent employee understands the patient-critical nature of our customers’ products.”

Accellent Inc. is a medical-device manufacturing and design company. It’s a subsidiary of Accellent Corp. For more information, visit www.accellent.com.

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For 40 years Quality Digest has been the go-to source for all things quality. Our newsletter, Quality Digest, shares expert commentary and relevant industry resources to assist our readers in their quest for continuous improvement. Our website includes every column and article from the newsletter since May 2009 as well as back issues of Quality Digest magazine to August 1995. We are committed to promoting a view wherein quality is not a niche, but an integral part of every phase of manufacturing and services.