483
Kabana Skin CareKabana Skin Care – FDA 483, Feb 20, 2025
Record Details
KABANA SKIN CARE, an OTC manufacturer in Louisville, CO, was cited with seven observations during an FDA inspection. The firm demonstrated a severe lack of fundamental quality control systems, including the absence of a quality control unit, inadequate written procedures for manufacturing and testing, and a failure to validate processes and equipment. These deficiencies indicate significant non-compliance with cGMP regulations, impacting product identity, strength, quality, and purity.
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ID · 8c65dbef-5b4d-4164-b259-53c4a724d349
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