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  7. Cambridge Isotope Laboratories, Inc.
483
•Cambridge Isotope Laboratories, Inc.•August 30, 2022

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.

Company
Cambridge Isotope Laboratories, Inc.
Inspection date
August 30, 2022
Product type
drugs
Office
Division of Northeast Imports 
Person
  • Robert J. Martin
View Company Profile

ID · 3ec74dfe-9d37-40af-8425-fe62bebcfaaf

Other documents for Cambridge Isotope Laboratories, Inc.
  • 483 - 2016-03-25March 25, 2016

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