Device Assembly
AFP assembles components to form ultra-high-quality analytical and diagnostic sub-assemblies. These products are manufactured under strict quality standards, such as ISO 13485, in FDA-registered facilities. AFP’s data collection and tracking methodologies are key elements in its world-class quality system. Every part is 100% tested and its production history is continuously recorded to ensure traceability and regulatory compliance.
AFP’s solutions include the following:
Sub-assembly: AFP produces smaller, functional units for later integration into complete analytical and diagnostic systems. These sub-assemblies can include mechanical, electrical, fluidic, or optical components. Our best-practice manufacturing system offers precision machining, laser welding or bonding, overmolding and insert molding, adhesive bonding and UV curing, and clean room assembly in its sub-assembly services.
Electro-mechanical assembly: AFP integrates mechanical components with electrical and electronic systems to create functional sub-assemblies. This process is critical for producing complex, high-reliability products such as analytical and diagnostic equipment. AFP’s integration capabilities include sensors and PCB integration, cable and connector assemblies, and motorized actuation units.
Clean room assembly: AFP offers in-house, controlled-environment assembly to ensure contamination-free products meet stringent regulatory and quality standards. Assembly occurs in our ISO Class 7 and Class 8 clean rooms.
White room assembly: AFP provides highly controlled, clean environments designed to minimize contamination during sensitive component assembly. Similar to clean room assembly, we provide a specific area with strict cleanliness protocols for assembling sterile or semi-sterile products.