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FDA Inspection
•Qilu Pharmaceutical Co., Ltd.•July 1, 2010

Qilu Pharmaceutical Co., Ltd. – FDA Inspection, Jul 1, 2010

Record Details

This FDA Inspection record concerns Qilu Pharmaceutical Co., Ltd., with an inspection on July 1, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Qilu Pharmaceutical Co., Ltd.
Inspection Date
July 1, 2010
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 5bab62d0-f575-4c47-b5b0-dc24e296c665

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
674203
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
September 23, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 25, 2013NAICenter 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 989208 - 2016-09-23
  • FDA Inspection 855751 - 2013-10-25

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