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483
•ABC Pharmaceuticals

ABC Pharmaceuticals – FDA 483

Record Details

Revance Therapeutics, Inc. in Newark, CA, a drug substance and drug product manufacturer, was inspected by the FDA. The inspection revealed significant deficiencies in cell bank testing, manufacturing process control, quality unit oversight of outsourced activities, yield determination, and written procedures for quality control. These issues indicate a lack of robust quality systems and process control, potentially impacting product quality and regulatory compliance.

Company
ABC Pharmaceuticals
Product type
drugs
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
People
  • Joao Pedras-Vasconcelos
  • Carla J. Lundi (Senior Consumer Safety Officer)
View Company Profile

ID · ee3e1027-7dbf-44b5-bf68-32a204281486

Other documents for ABC Pharmaceuticals
  • 483 - 2025-02-27February 27, 2025
  • EIR - 2022-07-15July 15, 2022
  • 483 - 2022-07-15July 15, 2022
  • 483 - 2021-07-02July 2, 2021

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