FDA Inspection 794437 — Zhejiang Hisun Pharmaceutical Co., Ltd.

Zhejiang Hisun Pharmaceutical Co., Ltd. — FEI 3007719313

The FDA completed an inspection of Zhejiang Hisun Pharmaceutical Co., Ltd. on Jul 19, 2012 in Taizhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jul 19, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Taizhou (China)

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