Continuous Improvement & Quality Certifications
ISO 13485 Certified Contract Manufacturer
Vonco Manufacturing Facilities
As an ISO 13485 certified contract manufacturer (Trevor, WI, Geneva, IL and Fortville, IN facilities), Vonco maintains the following quality standards, registrations, and certifications:
- ISO 13485 Certificate
- Medical Device Quality System Regulation 21 CFR 820
- FDA Registration
Quality and Excellence in Plastics Manufacturing
A dedication to continuous improvement is at the foundation of Vonco's success. Employees at each level of the organization — from machine operators to the CEO —are responsible for contributing to the improvement of the quality system and are empowered and trained as front-line inspectors in each phase of the manufacturing process.
Quality Committee
Our Quality Committee is responsible for managing the overall effectiveness of the Vonco Quality System, including review of critical continuous improvement activities (CAPA), customer complaints and audits. Members of the committee include the president and management representatives from Quality, Operations, Engineering and Production departments.
Quality Audits
If you’re considering our services, we encourage you to inquire about our quality audits. We proudly provide our customers with complete transparency into the manufacturing process.
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