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FDA Inspection
•Novartis Pharmaceuticals Corporation•April 7, 2017

Novartis Pharmaceuticals Corporation – FDA Inspection, Apr 7, 2017

Record Details

This FDA Inspection record concerns Novartis Pharmaceuticals Corporation, with an inspection on April 7, 2017, issued by the New Jersey District Office, covering biologics.

Company
Novartis Pharmaceuticals Corporation
Inspection Date
April 7, 2017
Product Type
Biologics
Office
New Jersey District Office
People
  • Ashley J. Burns (Issuing Officer)
  • Joan Johnson (Investigator)
  • Randa Melhem (Company Rep)
View Company Profile

ID · 9ab30769-64e6-41c7-bcc0-e04710bf5034

Inspection Facts

Inspection number
1019194
FDA center
Biologics
Outcome
Form 483 issued

Other FDA inspections of Novartis Pharmaceuticals Corporation

4
DateClassificationOfficeProject area
February 6, 2026Not classifiedNew Jersey District OfficeHuman Cellular, Tissue, and Gene Therapies
August 8, 2024VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
December 9, 2022NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
August 21, 2019VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Novartis Pharmaceuticals Corporation
  • FDA Inspection 1300144 - 2026-02-06
  • FDA Inspection 1245942 - 2024-08-08
  • FDA Inspection 1194474 - 2022-12-09
  • FDA Inspection 1100101 - 2019-08-21

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