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FDA Inspection
•Shandong Keyuan Pharmaceutical Co., Ltd.•August 2, 2018

Shandong Keyuan Pharmaceutical Co., Ltd. – FDA Inspection, Aug 2, 2018

Record Details

This FDA Inspection record concerns Shandong Keyuan Pharmaceutical Co., Ltd., with an inspection on August 2, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Shandong Keyuan Pharmaceutical Co., Ltd.
Inspection Date
August 2, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Shelby N. Turner (Investigator)
View Company Profile

ID · 165ba864-3231-419e-94b0-f03f7b3a3d50

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1064715
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Shandong Keyuan Pharmaceutical Co., Ltd.

2
DateClassificationOfficeProject area
June 14, 2024NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 10, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Shandong Keyuan Pharmaceutical Co., Ltd.
  • FDA Inspection 1244249 - 2024-06-14
  • FDA Inspection 927100 - 2015-04-10

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