FDA Investigator: Zi-Qiang Gu
- Zi-Qiang Gu first started conducting FDA inspections in 2004, with the last inspection in 2008. Over that time, Zi-Qiang Gu has conducted 12 inspections at 12 companies across 12 sites.
Get Zi-Qiang Gu's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.
Documents
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FDA 483 Shanghai No. 1 Biochemical & Pharmaceutical Co., Ltd., Shanghai | 2008
Out-of-stock
Zi-Qiang Gu
Human Drug Form 483
FDA 483 Qingdao Jiulong Biopharmaceutical Co., Qingdao, | 2008
Out-of-stock
Zi-Qiang Gu
Human Drug Form 483
FDA 483 Wuhan Shiji Jingmao Corp., Wuhan, Hubei | 2006
Out-of-stock
Zi-Qiang Gu
Human Drug Form 483
FDA 483 Yangzhou Pharmaceutical Ltd, Yangzhou, Jiangsu | 2006
Out-of-stock
Zi-Qiang Gu
Human Drug Form 483
FDA 483 Shanghai Medicinal Ltd. No. 15 Pharmaceutical Factory, Shanghai | 2005
Out-of-stock
Zi-Qiang Gu
Animal Drugs & Feed Form 483
FDA 483 Yunnan Hande Bio-Tech Co., Ltd., Kunming | 2004
Out-of-stock
Zi-Qiang Gu
Human Drug Form 483