483
LiquidCapsule Manufacturing, LLCLiquidCapsule Manufacturing, LLC – FDA 483, Feb 9, 2024
Record Details
LiquidCapsule Manufacturing, LLC in Tampa, FL, was cited for significant deficiencies in its manufacturing and quality control processes for OTC drug products. The inspection revealed a lack of fundamental procedures, including process and cleaning validation, equipment qualification, and adequate quality unit oversight. These issues indicate a severe lack of control over product quality, identity, strength, and purity.
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ID · 2e3d13c5-3ffd-43f6-b9bd-41710ce1428d
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