At JE Petersen, we pride ourselves on quality. We believe that a culture of excellence is the most important component of a medical device manufacturer. We strive daily to provide the highest quality products and services to our customers.
Quality Policy THE OBJECTIVE OF JE PETERSEN IS TO PROVIDE QUALITY PRODUCTS AND SERVICES THAT MEET THE NEEDS AND EXPECTATIONS OF OUR CUSTOMERS, PARTNERS, AND REGULATORY BODIES. WE OPERATE IN AN ENVIRONMENTALLY RESPONSIBLE AND SUSTAINABLE MANNER. WE ARE COMMITTED TO MEETING ALL APPLICABLE REQUIREMENTS AND CONTINUALLY IMPROVING THE EFFECTIVENESS OF THE QUALITY MANAGEMENT SYSTEM.
JE Petersen is an FDA registered manufacturer, fully compliant with all FDA 21 CFR 820 requirements.
JE Petersen has been assessed and certified to ISO 13485:2016 in respect of scope of operations given below:
Contract Manufacturing, Distribution and Servicing of Active Medical Systems for Neurological Diagnostics, Active and Non-Active Surgical Instruments for Plastic, Orthopedic, Thoracic and General Surgery.
JE Petersen is committed to producing high-quality products in a safe and environmentally sustainable manner.
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