483
Cambridge Isotope Laboratories, Inc.Cambridge Isotope Laboratories, Inc. – FDA 483, Aug 30, 2022
Record Details
Cambridge Isotope Laboratories, Inc. in Andover, MA, an Active Pharmaceutical Ingredient Manufacturer, was cited for a significant quality control issue. The firm failed to adequately investigate an out-of-specification result for Loss on Drying (LOD) during accelerated stability studies for Urea (C13, 99%). This failure involved not evaluating the potential impact on long-term stability data or the container closure system, instead prematurely concluding the bottle was unsuitable.
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