FDA Inspection 896935 — Zhejiang Lepu Pharmaceutical Co., Ltd.

Zhejiang Lepu Pharmaceutical Co., Ltd. — FEI 3004414647

The FDA completed an inspection of Zhejiang Lepu Pharmaceutical Co., Ltd. on August 29, 2014 in Taizhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 29, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Taizhou (China)