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FDA Inspection
•Rubicon Research Private Limited•March 8, 2024

Rubicon Research Private Limited – FDA Inspection, Mar 8, 2024

Record Details

This FDA Inspection record concerns Rubicon Research Private Limited, with an inspection on March 8, 2024, issued by the Center for Drug Evaluation and Research.

Company
Rubicon Research Private Limited
Inspection Date
March 8, 2024
Office
Center for Drug Evaluation and Research
Person
  • Camerson E. Moore (FDA Associated Person)
View Company Profile

ID · f00f8404-7177-4b65-bf89-298c4f087c92

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1231826
FDA center
Human Drugs
Project area
New Drug Evaluation

FDA Citations

1
  1. 21 CFR 211.67(a)Cleaning / Sanitizing / Maintenance

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Rubicon Research Private Limited

6
DateClassificationOfficeProject area
November 7, 2024NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
January 27, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 30, 2019VAIOffice of Inspections and InvestigationsGeneric Drug Evaluation
November 20, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 13, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Rubicon Research Private Limited
  • FDA Inspection 1250746 - 2024-11-07
  • FDA Inspection 1195651 - 2023-01-27
  • FDA Inspection 1102226 - 2019-08-30
  • FDA Inspection 1038536 - 2017-11-20
  • FDA Inspection 924394 - 2015-03-13

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