Copyright © 2010 All rights reserved Freije Quality Engineering, LLC
Veteran Owned Business
Freije Quality Engineering can assess your company’s adherence to FDA and ISO requirements.
We can evaluate your procedures, processes, and records to generate a detailed gap
analysis identifying your strengths and weaknesses.
After conducting the gap analysis your company will receive cost-effective recommendations
customized to the need of your company.
We do not believe in the one size fits all mentality.
We have developed a very thorough checklist that follows the FDA’s Quality System
Inspection Technique (QSIT) guide used by the FDA when they conduct facility inspections.