XLENT ACAI is produced under climate-controlled conditions in FDA-inspected facilities operating under Federal Good Manufacturing Practices (GMPs).
It is produced from a precise pilot blend which is then converted into our Master Batch Formula.The Master Batch Formula is comprised of a 15 page report detailing the specifics of each and every ingredient used.
Following the Master Formula, each ingredient is weighed, tagged, and placed in a separate container from each other ingredient. As each ingredient is weighed, both the operator and supervisor must sign off on the master batch record. This double signoff is repeated again when each ingredient is added to the blender. As a final step, the tags from each ingredient are tallied to eliminate any possibility of error.
In-process, capsules are -weighed every ten minutes by quality control technicians to certify that all products are of uniform in weight for a consistent dosage. If a capsule is off by more then the assigned target weight, manufacturing ceases, and solution is determined, this is repeated EVERY 10 MINUTES.
Once a lot number from the Master Batch Record has been encapsulated , capsules are then polished and spot checked. This process will identify partially filled capsules and or damaged capsules, these capsules will be removed from the production and dispensed, thus assuring you receive a uniform a 100% filled capsule.
