FDA Inspection
Jiangxi Synergy Pharmaceutical, Co., Ltd.Jiangxi Synergy Pharmaceutical, Co., Ltd. – FDA Inspection, Jan 10, 2019
Record Details
This FDA Inspection record concerns Jiangxi Synergy Pharmaceutical, Co., Ltd., with an inspection on January 10, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.
View Company Profile
ID · 860afe5f-1f7c-4561-9a5d-fb6d947ffb81
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1078075
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Jiangxi Synergy Pharmaceutical, Co., Ltd.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 7, 2025 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 9, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 9, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 11, 2009 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Jiangxi Synergy Pharmaceutical, Co., Ltd.
- FDA Inspection 1280670 - 2025-08-07
- FDA Inspection 996538 - 2016-09-09
- FDA Inspection 881487 - 2014-05-09
- FDA Inspection 614643 - 2009-09-11
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.