FDA Inspection 712157 — Zhejiang Huahai Pharmaceutical

Zhejiang Huahai Pharmaceutical — FEI 3003885745

The FDA completed an inspection of Zhejiang Huahai Pharmaceutical on Sep 8, 2010 in Linhai. 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
Sep 8, 2010
Fiscal Year
2010
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.