JUPITER, FL March 01, 2016 – Jenoptik Optical Systems, LLC. (JOSI) is pleased to announce the registration of its Quality Management System to ISO-13485:2003 for Medical Device manufacturers or service providers. The certification covers both design and manufacture of medical devices.
The company successfully obtained the registration through Intertek on its first audit attempt, complementing existing registrations to ISO 9001:2008. JOSI completed the audit in late January, 2016 and received the official certificate of registration in March, 2016.
“JOSI has a history of providing reliable, cost effective products to a highly regulated customer base. In addition, with manufacturing locations worldwide, Jenoptik allows for immediate access to high quality, low cost components. JOSI also offers vertical integration of optical design, manufacturing and system testing. Achieving this milestone is a tribute to our team and its commitment to growth in diagnostic instruments for life sciences,” remarks, Jay Kumler, President of Jenoptik Optical Systems. “This registration paves the way for expansion into medical markets where exceeding customer and regulatory expectations is a prerequisite,” said, John Racette, JOSI Quality Director.