FDA Inspection 1338934 — Zhejiang Wild Wind Pharmaceutical Co., Ltd.

Zhejiang Wild Wind Pharmaceutical Co., Ltd. — FEI 3006230668

The FDA completed an inspection of Zhejiang Wild Wind Pharmaceutical Co., Ltd. on Sep 11, 2026 in Dongyang. 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 11, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dongyang (China)

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