We offer a wide range of device assembly capabilities including design of custom made assembly tools, packaging, and sterilization services.
ISO 8 Cleanroom
Our Quality Management System is currently structured to meet the applicable requirements of 21 CFR 820 and 21 CFR 211 (ISO 13485:2016 in process).
We offer manufacturing document services including: specifications, Standard Operating Procedures, test methods, in process QC Inspection forms, Batch Records, etc. to meet your specific needs.