FDA Inspection 1101264 — Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API).

Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API). — FEI 3003663256

The FDA completed an inspection of Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API). on August 23, 2019 in Xianju. 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
August 23, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Xianju (China)