It is important for consumers (and the FDA) how a company manufactures and produces their products. As a company, ASEA greatly cares about strictly following the guidelines made by the FDA. They are cautious to stay up to date with any changes in regulations for manufacturing practices, so they can ensure their consumers
The NSF International is a global public health and safety organization that provides food safety and quality assurance services across all food supply chain sectors. They reviewed ASEA’s manufacturing process and certified their production center as a GMP (Good Manufacturing Practices) compliant facility.
Since ASEA Redox Supplement, is classified as a dietary supplement, the FDA doesn’t approve of it, however they regulate it. The FDA oversees dietary supplements under a different set of regulations. These regulations are different from those that cover conventional foods and drug products.
Before any company can distribute or market their product, they are responsible to making sure that the product in manufactures is safe and that there are no claims about the product that are false or misleading. The product must also comply with the Federal Food, Drug and Cosmetic Act and FDA regulations in all other ways. These laws cover topical supplements (like RENU 28) as well as foods and supplements.
ASEA has invested millions of dollars into a 41,500 square foot production facility that has testing labs, a large production area, and offices. In these buildings roughly 15,000 cases of ASEA Redox Supplement and 10,000 tubes of RENU 28 are produced each week. This is only about 30% of the facilities capacity, which allows a lot of room for growth as the company continues to expand and grow. Something else that makes ASEA’s facility unique is that since it is theirs, they get 100% say on how they are going to operate their manufacturing process. It allows them to maintain a high quality assurance, control costs, and provide stability to their business.