FDA Inspection 717785 — Shenzhen Hepalink Pharmaceutical Co., Ltd.

Shenzhen Hepalink Pharmaceutical Co., Ltd. — FEI 3002808210

The FDA completed an inspection of Shenzhen Hepalink Pharmaceutical Co., Ltd. on January 27, 2011 in Shenzhen. 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
January 27, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Shenzhen (China)