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FDA Inspection
•Raybow (Suzhou) Pharmaceutical Co., Ltd.•September 19, 2014

Raybow (Suzhou) Pharmaceutical Co., Ltd. – FDA Inspection, Sep 19, 2014

Record Details

This FDA Inspection record concerns Raybow (Suzhou) Pharmaceutical Co., Ltd., with an inspection on September 19, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Raybow (Suzhou) Pharmaceutical Co., Ltd.
Inspection Date
September 19, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 54ea1ec1-bcb1-4e23-a9f5-c6ba7be77b0e

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
910769
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Raybow (Suzhou) Pharmaceutical Co., Ltd.

3
DateClassificationOfficeProject area
May 22, 2025Not classifiedOffice of Inspections and Investigations
October 18, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 25, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Raybow (Suzhou) Pharmaceutical Co., Ltd.
  • FDA Inspection 1273595 - 2025-05-22
  • FDA Inspection 1071681 - 2018-10-18
  • FDA Inspection 671664 - 2010-05-25

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