VistaMed is committed to achieving 100% customer satisfaction through the rigorous application of ISO 13485:2003. VistaMed’s Quality System also takes account the European Medical Device Directive 93/42 – EEC and also the FDA’s QSR – 21 CFR Part 820. The policy of our dedicated Quality assurance team is to achieve total customer satisfaction by supplying defect free products.
At VistaMed, we continually review our performance to ensure that our quality system remains effective and are constantly striving for improvement.
VistaMed is dedicated to working with our customers to achieve their quality objectives. Our experienced Quality department is able to assist you in compiling a technical file and CE marking your proprietary products.
FDA registration number: 3008328690