FDA Inspection 882356 — Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.

Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd. — FEI 3004944662

The FDA completed an inspection of Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd. on May 16, 2014 in Dongyang. 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
May 16, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dongyang (China)