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FDA Inspection
•Jiangxi Synergy Pharmaceutical, Co., Ltd.•September 9, 2016

Jiangxi Synergy Pharmaceutical, Co., Ltd. – FDA Inspection, Sep 9, 2016

Record Details

This FDA Inspection record concerns Jiangxi Synergy Pharmaceutical, Co., Ltd., with an inspection on September 9, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Jiangxi Synergy Pharmaceutical, Co., Ltd.
Inspection Date
September 9, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · b8e66a8e-136e-49ea-ac40-542f530683f8

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
996538
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
May 9, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 11, 2009VAICenter 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 881487 - 2014-05-09
  • FDA Inspection 614643 - 2009-09-11

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