JE Petersen Achieves 13485:2016
JE Petersen’s commitment to quality has led to the company re-certifying to the newest standard for medical device manufacturers, ISO 13485:2016. This new standard has many changes and upgrades, most notably in the areas of risk management and process validation. The scope of our certificate is as follows: “Contract Manufacturing, Distribution, and Servicing of Active
JE Petersen Upgrades Its Dermatome Repair Center
March 24, 2017 – JE Petersen is proud to announce a major redesign to our Padgett Dermatome Repair Center, the only authorized repair center in the United States for Integra Padgett Dermatomes. Our newly redesigned quality department features environmental isolation and control, real-time 24/7 environmental monitoring, and improved traceability of environmental factors. The new quality
About Our Name Change
Dadson Manufacturing Corporation was founded in 1988 by father and son, James and Bill Petersen. With Bill’s retirement in 2002, and James’ passing in 2006, the “Dad” and “Son” in our name were no longer part of the daily operation. With that in mind, we have decided to honor Jim Petersen by doing business as
JE Petersen Achieves RoHS II Compliance
April 3, 2015 – After many months of effort, JE Petersen is now fully compliant with 60601-1 3rd Edition including RoHS compliance. JE Petersen is committed to producing high-quality products in a safe and environmentally sustainable manner.
JE Petersen Achieves ISO Certification
November 2, 2009 – JE Petersen is proud to announce it has attained ISO 9001 and ISO 13485 Certifications. We are committed to quality and the continuous improvement of our quality system and our products.