GF Health Products, Inc. is committed to full FDA compliance. All of its factories, suppliers and products, meet CFR 21, Parts 820.

21 CFR, Part 820 is the Quality System Regulation Medical Device Manufacturers

21 CFR Part 820, also known as the Quality System Regulation QSR outlines Current Good Manufacturing Practice CGMP regulations that govern the methods used in, and the facilities and controls used for, the design, manufacture, packaging, labeling, storage, installation, and servicing of all finished devices intended for human use. These requirements are meant to ensure that medical devices are safe and effective. Medical device manufacturers undergo FDA inspections to ensure QSR compliance.