FDA Inspection 875391 — Zhejiang Jiangbei Pharmaceutical Co., Ltd.

Zhejiang Jiangbei Pharmaceutical Co., Ltd. — FEI 3004986814

The FDA completed an inspection of Zhejiang Jiangbei Pharmaceutical Co., Ltd. on April 3, 2014 in Taizhou City. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 3, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Taizhou City (China)