FDA Inspection 742581 — Zhejiang Haizhou Pharmaceutical Co., Ltd.

Zhejiang Haizhou Pharmaceutical Co., Ltd. — FEI 3002917378

The FDA completed an inspection of Zhejiang Haizhou Pharmaceutical Co., Ltd. on June 30, 2011 in Linhai. 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
June 30, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Linhai (China)