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FDA Inspection
•Gedeon Richter Plc., Dorog Site•February 8, 2019

Gedeon Richter Plc., Dorog Site – FDA Inspection, Feb 8, 2019

Record Details

This FDA Inspection record concerns Gedeon Richter Plc., Dorog Site, with an inspection on February 8, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Gedeon Richter Plc., Dorog Site
Inspection Date
February 8, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • MRA DavisM (Issuing Officer)
View Company Profile

ID · cc030db1-91b1-4f34-a732-2d568a697099

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1099017
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Gedeon Richter Plc., Dorog Site

4
DateClassificationOfficeProject area
October 17, 2024Not classifiedOffice of Inspections and Investigations
January 29, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 24, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 12, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Gedeon Richter Plc., Dorog Site
  • FDA Inspection 1272329 - 2024-10-17
  • FDA Inspection 960344 - 2016-01-29
  • FDA Inspection 844606 - 2013-05-24
  • FDA Inspection 741959 - 2011-07-12

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