FDA Inspection 1062283 — Zhejiang Huahai Pharmaceutical

Zhejiang Huahai Pharmaceutical — FEI 3003885745

The FDA completed an inspection of Zhejiang Huahai Pharmaceutical on Aug 3, 2018 in Linhai. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Aug 3, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Linhai (China)

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