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FDA Inspection
•Jilin Shulan Synthetic Pharmaceutical Co. Ltd.•March 20, 2015

Jilin Shulan Synthetic Pharmaceutical Co. Ltd. – FDA Inspection, Mar 20, 2015

Record Details

This FDA Inspection record concerns Jilin Shulan Synthetic Pharmaceutical Co. Ltd., with an inspection on March 20, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Jilin Shulan Synthetic Pharmaceutical Co. Ltd.
Inspection Date
March 20, 2015
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · ae318d36-cad5-4158-8b7b-7a2f5d5c59ae

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
921290
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Jilin Shulan Synthetic Pharmaceutical Co. Ltd.

3
DateClassificationOfficeProject area
November 10, 2017OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 30, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 28, 2009OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Jilin Shulan Synthetic Pharmaceutical Co. Ltd.
  • FDA Inspection 1032074 - 2017-11-10
  • FDA Inspection 755260 - 2011-11-30
  • FDA Inspection 612640 - 2009-08-28

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