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FDA Inspection
•Laboratorios Rubio S.A.•June 23, 2017

Laboratorios Rubio S.A. – FDA Inspection, Jun 23, 2017

Record Details

This FDA Inspection record concerns Laboratorios Rubio S.A., with an inspection on June 23, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Laboratorios Rubio S.A.
Inspection Date
June 23, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Seongeun Cho (Issuing Officer)
  • Sripal R. Mada (Company Rep)
View Company Profile

ID · 3713028b-06f1-457b-aada-bd9e1fb2afb9

Inspection Facts

Inspection number
1032027
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Laboratorios Rubio S.A.

4
DateClassificationOfficeProject area
September 22, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 31, 2019VAICenter for Drug Evaluation and ResearchBioresearch Monitoring
June 18, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 30, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Laboratorios Rubio S.A.
  • FDA Inspection 1262693 - 2022-09-22
  • FDA Inspection 1115466 - 2019-10-31
  • FDA Inspection 1160057 - 2019-06-18
  • FDA Inspection 1021743 - 2017-06-30

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