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483
•Novartis Gene Therapies, Inc.•August 2, 2019

Novartis Gene Therapies, Inc. – FDA 483, Aug 2, 2019

Record Details

AveXis, Inc. in San Diego, CA, a control testing lab, was cited for significant deficiencies during an FDA inspection. The firm failed to thoroughly investigate unexplained discrepancies, maintain complete laboratory records, and ensure proper quality control unit responsibilities. Additionally, issues were noted with the testing and standardization of reference standards and adherence to established test procedures, indicating systemic quality control and data integrity concerns.

Company
Novartis Gene Therapies, Inc.
Inspection date
August 2, 2019
Product type
biologics
Office
Division of Pharmaceutical Quality Operations IV
People
  • Mihaly S. Ligmond (CSO)
  • Scott T. Ballard
View Company Profile

ID · 85c00fe0-e2f3-427e-80bc-ff47ccffb85a

Violation Codes3
21 CFR 331(c)21 U.S.C. 324(a)(4)FD&C Act 905(j)

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Other documents for Novartis Gene Therapies, Inc.
  • 483 - 2021-08-23August 23, 2021
  • EIR - 2019-02-15February 15, 2019

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