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FDA Inspection
•Shandong Keyuan Pharmaceutical Co., Ltd.•April 10, 2015

Shandong Keyuan Pharmaceutical Co., Ltd. – FDA Inspection, Apr 10, 2015

Record Details

This FDA Inspection record concerns Shandong Keyuan Pharmaceutical Co., Ltd., with an inspection on April 10, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Shandong Keyuan Pharmaceutical Co., Ltd.
Inspection Date
April 10, 2015
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · aaf4e02c-e992-459b-8c01-d0358a14b273

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
927100
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
August 2, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Shandong Keyuan Pharmaceutical Co., Ltd.
  • FDA Inspection 1244249 - 2024-06-14
  • FDA Inspection 1064715 - 2018-08-02

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