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483
•Veranova LP•February 15, 2023

Veranova LP – FDA 483, Feb 15, 2023

Record Details

An FDA inspection of Veranova, L.P. in West Deptford, NJ, revealed significant deficiencies in their quality system. The firm failed to adequately investigate customer complaints regarding inaccurate API documentation and implement effective corrective actions. Additionally, the inspection found that the company lacked sufficient written procedures for cleaning validation of non-dedicated manufacturing equipment, with a related CAPA remaining open for an extended period.

Company
Veranova LP
Inspection date
February 15, 2023
Product type
drugs
Office
New Jersey District Office
People
  • Amy N. Chen (Investigator)
  • Karen A. Briggs (Investigator)
  • Kristina L. Conroy (Investigator)
  • Rachael O. Oyewole
View Company Profile

ID · 5c9511c0-1673-490a-9186-91cbf8b6d26a

Other documents for Veranova LP
  • 483 - 2026-01-23January 23, 2026
  • EIR - 2023-03-15March 15, 2023
  • 483 - 2019-03-08March 8, 2019

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