More than just a part of the manufacturing process, quality assurance is the benchmark for success at Plastek. It is built into every aspect of operations and every job function company wide.

All of our manufacturing facilities are ISO 9002 certified or currently working towards ISO certification. This insures a comprehensive quality assurance program throughout the entire manufacturing cycle. In order to success in the quality process of our customers products, every employee at Plastek follows controlled procedures, work instructions, visual standards and quality plans to produce plastic injection molded parts that will meet or exceed the expectations of the customer.

Plastek is committed to producing zero defects. The quality of any part depends on the quality of the material used. Every lot of resin delivered to Plastek is put through a comprehensive series of tests in our onsite materials lab before we accept it for production. This includes ASTM standard test methods such as melt flow, tensile and density tests. In addition, we perform other product specific tests developed by Plastek Quality Engineering for such things as moisture content and color leaching.

Plastek produces various types of pharmaceutical assemblies and components to meet the needs of laboratories, hospitals, physicians and over the counter applications. Plastek is registered with the FDA as a medical device manufacturer and can be found on their drug master file. Products are made under strict regulations, policies and procedures following GMP guidelines (Good Manufacturing Practice) to insure our customers receive a product, which meets or exceeds FDA requirements. Plastek can also provide molding, decorating and assembly in our clean room facility.

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