FDA Drug Establishment Registration
In July, 2011, USANA’s in-house facility gained Drug Establishment Registration with the U.S. Food and Drug Administration (FDA).
Operating an FDA-registered facility brings with it an increased amount of scrutiny. While other companies are required to follow the FDA’s less stringent nutritional supplement standards, USANA’s facilities can and will be inspected by the FDA under pharmaceutical guidelines—the FDA’s highest possible standard for manufacturers. Every step of the manufacturing process—from the handling of raw materials to tabletting—is required to comply with these strict guidelines.
USANA has been voluntarily adhering to these exacting standards for years. Our compliance with pharmaceutical-grade Good Manufacturing Practices (GMPs) means no changes will need to be made to the manufacturing processes in order to comply with the increased FDA scrutiny. The Drug Establishment Registration simply makes official something Associates and customers have always known.
The FDA registration is another statement of USANA’s unwavering confidence in the quality of its products—a statement you can happily share with your family, friends, neighbors, and Potential Associates/Customers.
Last modified: September 24, 2020
