Versa Electronics Completes ISO 9001:2015 Transition and Achieves ISO 13485:2003 Registration
In accordance with ISO 9001:2015, and based on the recently completed assessment by our registrar, Orion Registrar, Inc. (“Orion”), Versa Electronics is on the leading edge of a group of companies that have completed the transition to the new ISO 9001:2015 standard in 2017. Many of Orion’s customers have decided to wait another year before attempting the transition. This achievement continues to demonstrate the kind of quality organization Versa provides its industrial clients.
Versa Electronics has a long history of producing medical devices and sub-assemblies. Versa’s services to the Medical Device OEM market includes the supply of Printed Circuit Assemblies, Wire Harness/Cable Assemblies, and Electronic Sub-assemblies. Kurt Orr, Versa Sales Manager, addressed the fact that the ISO 13485 certification is not a requirement to provide these services. In so doing Kurt was excited to say, “Versa Electronics wanted to show our current medical device customers and the medical device community our ongoing commitment to continuous improvement by achieving ISO 13485:2003!!”
Bill Jackson, Versa Electronics Quality Manager, reports that Versa’s Quality Management System and addition of ISO 13485 opens the potential market to over 602 establishments in Minnesota alone. This note further enhances our longstanding FDA registration and is directly in line with Versa’s EMS growth objectives.
About Versa Electronics
Versa Electronics is a privately held Electronic Contract Manufacturing Services company based in suburban Minneapolis, MN. Versa has 24 years of providing manufacturing and design services to OEM’s of medical, utility and power, communications, security, industrial and consumer products. Beyond Versa’s capabilities, their niche value to their clients is founded in the personal service and operational versatility, flexibility and proven product reliability results. Learn more at versae.com.
