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FDA Inspection
•Jiangxi Synergy Pharmaceutical, Co., Ltd.•September 11, 2009

Jiangxi Synergy Pharmaceutical, Co., Ltd. – FDA Inspection, Sep 11, 2009

Record Details

This FDA Inspection record concerns Jiangxi Synergy Pharmaceutical, Co., Ltd., with an inspection on September 11, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Jiangxi Synergy Pharmaceutical, Co., Ltd.
Inspection Date
September 11, 2009
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · bf561fc6-636e-4543-b625-bfb671b1bb46

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
614643
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Jiangxi Synergy Pharmaceutical, Co., Ltd.

4
DateClassificationOfficeProject area
August 7, 2025NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 10, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 9, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 9, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Jiangxi Synergy Pharmaceutical, Co., Ltd.
  • FDA Inspection 1280670 - 2025-08-07
  • FDA Inspection 1078075 - 2019-01-10
  • FDA Inspection 996538 - 2016-09-09
  • FDA Inspection 881487 - 2014-05-09

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