FDA Inspection 610604 — Zhejiang Hisoar Pharmaceutical Co. Ltd.

Zhejiang Hisoar Pharmaceutical Co. Ltd. — FEI 3003735151

The FDA completed an inspection of Zhejiang Hisoar Pharmaceutical Co. Ltd. on August 29, 2009 in Taizhou. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 29, 2009
Fiscal Year
2009
Product Type
Veterinary
Project Area
Pre-Approval Eval. of Animal Drugs and Food Additives
Location
Taizhou (China)