FDA Inspection 1013039 — Zhejiang Haisen Pharmaceutical Co., Ltd.

Zhejiang Haisen Pharmaceutical Co., Ltd. — FEI 3003967524

The FDA completed an inspection of Zhejiang Haisen Pharmaceutical Co., Ltd. on Apr 21, 2017 in Dongyang. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Veterinary.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Apr 21, 2017
Fiscal Year
2017
Product Type
Veterinary
Project Area
Pre-Approval Eval. of Animal Drugs and Food Additives
Location
Dongyang (China)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.