Facility Credentials
FDA Facility Registration
Designed Nutritional Products is registered with the U.S. Food and Drug Administration pursuant to Section 305 of the Public Health Security and Bioterrorism Preparedness and Response Act of 2002, P.L. 107-188.
Registration Number
14011365240
Effective Date
November 10, 2003
GMP Standard
21 CFR Part 117
Facility Location
Orem, Utah, USA
Registration Details
Official FDA Facility Registration
Designed Nutritional Products has registered with the U.S. Food and Drug Administration pursuant to Section 305 of the United States Public Health Security and Bioterrorism Preparedness and Response Act of 2002, P.L. 107-188, with registration submitted with the registrant's authorization by FDA Registrar Corp.
Official Registration Record
Designed Nutritional Products, Inc.
Registered Facility Designed Nutritional Products, Inc.
U.S. FDA Registration No. 14011365240
Effective Date of Registration November 10, 2003
Registered Under P.L. 107-188, Section 305
Facility Address 1199 South 1480 West, Orem, UT 84058
GMP Compliance Standard 21 CFR Part 117
Verification Available on request — contact us directly
What This Means for Your QA Program
What FDA registration and CFR 117 compliance means for buyers
FDA Registered Facility
FDA facility registration under the Bioterrorism Act confirms our facility is known to and on file with the FDA. This is a baseline requirement for food and dietary supplement manufacturers supplying the U.S. market.
21 CFR Part 117 Compliant
Current Good Manufacturing Practice regulations (21 CFR Part 117) govern how we manufacture, process, pack, and hold food and dietary supplement ingredients. Compliance means documented procedures, trained personnel, and verified quality controls.
Full Documentation
A Certificate of Analysis is provided with every order. Additional documentation including Safety Data Sheets, certificates of origin, and analytical method references are available on request for all products.
Verfied Testing
Every batch is tested against specifications before release. Germanium Sesquioxide undergoes multiple distinct analytical tests per batch. All products are warehoused and tested by Third-Parties before release..