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FDA Inspection
•Novartis Pharma Stein AG•August 24, 2017

Novartis Pharma Stein AG – FDA Inspection, Aug 24, 2017

Record Details

This FDA Inspection record concerns Novartis Pharma Stein AG, with an inspection on August 24, 2017, issued by the Office of Inspections and Investigations, covering biologics.

Company
Novartis Pharma Stein AG
Inspection Date
August 24, 2017
Product Type
Biologics
Office
Office of Inspections and Investigations
People
  • Debra M. Emerson (FDA Associated Person)
  • Susan M. Jackson (Issuing Officer)
View Company Profile

ID · f7f14324-13d3-44e9-802f-d55ecc1beaae

Inspection Facts

Inspection number
1025563
FDA center
Biologics
Outcome
Form 483 issued

Other FDA inspections of Novartis Pharma Stein AG

13
DateClassificationOfficeProject area
May 19, 2026Not classifiedOffice of Inspections and InvestigationsHuman Cellular, Tissue, and Gene Therapies
November 20, 2023Not classifiedOffice of Inspections and Investigations
December 6, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 4, 2018VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
September 21, 2018Not classifiedOffice of Inspections and Investigations
View all 13 other inspections on the company page
Other documents for Novartis Pharma Stein AG
  • FDA Inspection 1319902 - 2026-05-19
  • FDA Inspection 1230809 - 2023-11-20
  • FDA Inspection 1192104 - 2022-12-06
  • FDA Inspection 1073408 - 2018-12-04
  • FDA Inspection 1071638 - 2018-09-21

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