Innovite, Inc. is a registered facility with the U.S. Food and Drug Administration (# 15020127078) located in Sherwood Oregon, USA.
Built in 2017, this state-of-the-art facility features over 28,000 sq. ft. of production and warehouse space where we provide dry tableting, blending, and bottling capabilities.
Our manufacturing process – from receipt of raw materials to shipment of finished products – is in compliance with the current Good Manufacturing Practice (cGMP) for dietary supplements.
Our business is regulated by the FDA, which regularly audits our facility to ensure our manufacturing, packaging, labeling, and holding processes adhere to the strict cGMP standards.
By adhering to these high manufacturing standards, we can ensure the purity and potency of final products.
