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FDA Inspection
•BrightGene BioMedical Technology Co., Ltd.•August 10, 2023

BrightGene BioMedical Technology Co., Ltd. – FDA Inspection, Aug 10, 2023

Record Details

This FDA Inspection record concerns BrightGene BioMedical Technology Co., Ltd., with an inspection on August 10, 2023, issued by the Office of Inspections and Investigations.

Company
BrightGene BioMedical Technology Co., Ltd.
Inspection Date
August 10, 2023
Office
Office of Inspections and Investigations
Person
  • Niketa Patel (FDA Associated Person)
View Company Profile

ID · 49151401-67e1-4521-8c26-0dadf69aba27

Inspection Facts

Inspection number
1216401
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of BrightGene BioMedical Technology Co., Ltd.

1
DateClassificationOfficeProject area
September 9, 2026Not classifiedOffice of Inspections and Investigations
Other documents for BrightGene BioMedical Technology Co., Ltd.
  • FDA Inspection 1342072 - 2026-09-09

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