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483
•ABRYL LABORATORIES PRIVATE LIMITED•August 20, 2024

ABRYL LABORATORIES PRIVATE LIMITED – FDA 483, Aug 20, 2024

Record Details

Abryl Laboratories Private Limited, a sterile drug manufacturer in Dera Bassi, India, was cited for significant deficiencies in its quality control and manufacturing processes. Observations included a lack of scientifically sound sampling plans and test procedures, failure to thoroughly investigate non-viable particle excursions, and inadequate qualification of visual inspectors for drug product inspection. These issues indicate a lack of robust controls to ensure drug product quality and purity.

Company
ABRYL LABORATORIES PRIVATE LIMITED
Inspection date
August 20, 2024
Product type
drugs
Office
Foreign - CDER (Non-Bioresearch Monitoring)
People
  • Crystal Monroy
  • Gavin T. Cua (issuing_officer)
View Company Profile

ID · 4d31e593-ab87-4745-9424-c46d5017d2e6

Other documents for ABRYL LABORATORIES PRIVATE LIMITED
  • 483 - 2025-09-26September 26, 2025
  • 483 - 2023-11-20November 20, 2023
  • EIR - 2022-12-06December 6, 2022
  • 483 - 2022-12-06December 6, 2022
  • 483 - 2022-01-22January 22, 2022

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