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483
•Kabana Skin Care•February 20, 2025

Kabana 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.

Company
Kabana Skin Care
Inspection date
February 20, 2025
Product type
drugs
Office
Denver District Office
Person
  • Dogbeda F. Mackenzie
View Company Profile

ID · 8c65dbef-5b4d-4164-b259-53c4a724d349

Other documents for Kabana Skin Care
  • WARNING_LETTER - 2025-03-18March 18, 2025
  • WARNING_LETTER - 2025-02-20February 20, 2025

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