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483
•LiquidCapsule Manufacturing, LLC•February 9, 2024

LiquidCapsule 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.

Company
LiquidCapsule Manufacturing, LLC
Inspection date
February 9, 2024
Product type
drugs
Office
Office of Medical Device and Radiological Health Division II
People
  • Suzanne N. Vallez
  • Shelby N. Turner
  • Frederick H. Miller
View Company Profile

ID · 2e3d13c5-3ffd-43f6-b9bd-41710ce1428d

Other documents for LiquidCapsule Manufacturing, LLC
  • WARNING_LETTER - 2025-07-03July 3, 2025
  • 483 - 2025-07-03July 3, 2025
  • WARNING_LETTER - 2014-10-20October 20, 2014

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