FDA 483 - Deseret Laboratories, Inc. - March 23, 2018

Deseret Laboratories, Inc. in Saint George, UT, was inspected and received a Form 483 with four observations primarily concerning inadequate quality control and record-keeping practices. The firm failed to properly calibrate equipment, maintain complete batch production records, ensure adequate laboratory controls, and provide complete stability testing records for homeopathic drug products. These issues indicate significant deficiencies in their manufacturing and quality systems.