Precision ADM Continues to Invest in Quality Systems and Registrations to Fully Serve the Medical Device Industry
WINNIPEG, Manitoba (PRWEB) December 20, 2018 -- Precision ADM, Inc. (“Precision ADM” or "the Company"), a global engineering and metal additive manufacturing solutions provider, is pleased to announce that it has successfully completed FDA establishment registration for 2018/2019. This registration is required by the FDA for contract manufacturing facilities and individual devices.
“Along with our ISO 13485 certification,” said Derek VanDenDriessche, Director of Medical Sales, “this FDA Establishment Registration assures our customers that we are fully equipped for manufacturing complex medical devices using metal additive manufacturing technologies.”
“We’re very proud to be the only metal additive manufacturing service provider in Canada to hold ISO 13485 certification and FDA establishment registration,” added Martin Petrak, Chief Executive Officer. “This highlights our commitment to Quality Management Systems and to providing regulatory-approved devices to our clients."
For more information on manufacturing medical devices and other Additive Manufacturing solutions, please contact Precision ADM via email at: [email protected] or visit us online at: precisionadm.com
About Precision ADM Inc.
Precision ADM is a global engineering and manufacturing solutions provider that uses Additive Manufacturing, also known as 3D Printing, as a core technology, complimented by multi-axis machining to manufacture high value components and devices for the medical, aerospace, energy, and industrial sectors. Precision ADM has created a comprehensive Advanced Digital Manufacturing™ process which includes Design Support, Engineering, Manufacturing and Finishing. Precision ADM possesses ISO 13485:2016, AS9100 Rev D, and ISO 9001:2015 certifications and is headquartered in Winnipeg, Manitoba, Canada.
Graeme Findlay, Precision ADM, http://www.precisionadm.com, +1 204-289-4491 Ext: 216, [email protected]
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