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FDA Inspection
•Changzhou Yinsheng Pharmaceutical Co. Ltd.•May 13, 2016

Changzhou Yinsheng Pharmaceutical Co. Ltd. – FDA Inspection, May 13, 2016

Record Details

This FDA Inspection record concerns Changzhou Yinsheng Pharmaceutical Co. Ltd., with an inspection on May 13, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Changzhou Yinsheng Pharmaceutical Co. Ltd.
Inspection Date
May 13, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 5f1b687e-a4c3-4bd7-b78d-9ae914c65325

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
970587
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Changzhou Yinsheng Pharmaceutical Co. Ltd.

3
DateClassificationOfficeProject area
June 7, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 8, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 28, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Changzhou Yinsheng Pharmaceutical Co. Ltd.
  • FDA Inspection 1245862 - 2024-06-07
  • FDA Inspection 822230 - 2013-02-08
  • FDA Inspection 727443 - 2011-04-28

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