How Frunutta Ensures All Our Tablets Are the Highest Quality
Frunutta was founded by a father who needed to help his autistic son get his nutrients fast and efficiently. Since none of the other methods of absorbing vitamins were good solutions for his son, Dr. Alavi had no other option but to bring together a team of physicians and a nutraceutical expert to create the solution. After intensive research and rigorous testing, Frunutta was born.
Today these tiny, pure vitamins that quickly dissolve under the tongue have become the perfect solution for anyone who wants a clean, easy, fast and efficient way to take their dietary supplements. Our biggest fans are people with autism, those who want to live a non-toxic lifestyle, who have trouble swallowing vitamins and get stomach problems from them.
It is Frunutta’s mission to build on its legacy of innovation by providing the world with nutritionally enhanced products that support an energetic, healthy lifestyle.
Our State-of-the-Art Facility
Frunutta’s main NSF cGMP certified facility is based in Los Angeles, California. All manufacturing activities are carried out at this state-of-the-art facility site, from raw ingredients to bottling and packaging. We manufacture more than 20 different Micro Quick Absorb® Instant Dissolve Tablets. The supplements are mixed from raw ingredients, per individual formulations, and compiled by Current Good Manufacturing Practice (cGMP) trained staff with adherence to purity and high standards set by the Food and Drug Branch of the California Department of Public Health. Subsequently, all products are filled and packaged in strict accordance with cGMP.
Quality Management Systems
The organizational structure of the quality assurance system is based upon the implementation of cGMP. The Quality Control function is to ensure that the entire finished product is as defined above. On the other hand, the Quality Assurance function is to ensure that all raw ingredients comply with their individual specifications.
We undertake and carry out microbial, heavy metals, Gluten, GMO, assay, purity analysis, active ingredients analysis, and any other necessary tests on both raw ingredients and finished products to ensure that all products are of a high quality and in strict accordance with United States of America Food and Drug Administration legislation and guidelines.
Testing Methods and Laboratories
Frunutta vitamins test both raw materials and finished products with external, approved laboratories. These laboratories are carefully selected and must be ISO/IEC 17025 accredited and comply with the most rigid industry standards. This accreditation provides an objective third-party assessment of the managerial and technical competence of testing laboratories and assures the "precision, accuracy and traceability" analytical results are proficient data.
Frunutta is aware of impurity as a health risk to consumers. This is why, on top of the regular testing, we also occasionally have external audits carried out, and audits by State and Federal authorities are carried out biannually.
All in all, we are confident that our strict adherence to the defined manufacturing processes and quality control, independent microbial and purity analysis, help ensure that all Frunutta’s products are within US guidelines and standards, adherent to the purity of the finished goods that we promise.