483
Consumer Product Partners, LLCConsumer Product Partners, LLC – FDA 483, Jun 14, 2023
Record Details
Vi-Jon, LLC, a human drug manufacturer in Saint Louis, MO, was cited for significant deficiencies across four observations. The inspection revealed failures in preventing microbial contamination, thoroughly investigating discrepancies, adhering to quality unit responsibilities, and following procedures for component handling and testing. These issues indicate a systemic breakdown in quality control and manufacturing practices.
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ID · f9b13098-1fc9-4576-a704-2c6688de05fa
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