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FDA Inspection
•Qilu Pharmaceutical Co., Ltd.•September 23, 2016

Qilu Pharmaceutical Co., Ltd. – FDA Inspection, Sep 23, 2016

Record Details

This FDA Inspection record concerns Qilu Pharmaceutical Co., Ltd., with an inspection on September 23, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Qilu Pharmaceutical Co., Ltd.
Inspection Date
September 23, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 17c953fd-decb-49f5-988d-a7947f23b71f

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
989208
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Qilu Pharmaceutical Co., Ltd.

5
DateClassificationOfficeProject area
April 4, 2025Not classifiedOffice of Inspections and Investigations
February 22, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 9, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 25, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 1, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Qilu Pharmaceutical Co., Ltd.
  • FDA Inspection 1269032 - 2025-04-04
  • FDA Inspection 1088395 - 2019-02-22
  • FDA Inspection 1048729 - 2018-03-09
  • FDA Inspection 855751 - 2013-10-25
  • FDA Inspection 674203 - 2010-07-01

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