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FDA Inspection
•Sanofi Winthrop Industrie•March 22, 2019

Sanofi Winthrop Industrie – FDA Inspection, Mar 22, 2019

Record Details

This FDA Inspection record concerns Sanofi Winthrop Industrie, with an inspection on March 22, 2019, issued by the Office of Inspections and Investigations, covering biologics.

Company
Sanofi Winthrop Industrie
Inspection Date
March 22, 2019
Product Type
Biologics
Office
Office of Inspections and Investigations
People
  • Jacqueline M. Diaz Albertini (Company Rep)
  • Mihaly S. Ligmond (FDA Associated Person)
View Company Profile

ID · 9829daef-4445-43ea-8008-2b66b3b615fa

Inspection Facts

Inspection number
1089715
FDA center
Biologics
Outcome
Form 483 issued

Other FDA inspections of Sanofi Winthrop Industrie

6
DateClassificationOfficeProject area
September 15, 2026Not classifiedOffice of Inspections and InvestigationsVaccines and Allergenic Products
September 29, 2023VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
September 27, 2017Not classifiedOffice of Inspections and Investigations
September 25, 2015VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
June 21, 2013VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
View all 6 other inspections on the company page
Other documents for Sanofi Winthrop Industrie
  • FDA Inspection 1336872 - 2026-09-15
  • FDA Inspection 1221498 - 2023-09-29
  • FDA Inspection 1028373 - 2017-09-27
  • FDA Inspection 945414 - 2015-09-25
  • FDA Inspection 838673 - 2013-06-21

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