483
CBR Systems IncFDA 483 - CBR Systems Inc - June 03, 2009
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CBR Systems Inc, a cord blood/stem cell processor in Tucson, AZ, was cited for multiple deficiencies during an FDA inspection. Observations included inadequate processing to prevent contamination, unvalidated procedures for handling exposed products, insufficient donor screening for communicable diseases, and a lack of proper environmental monitoring for microorganisms.
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