FDA Inspection 1261674 — Zhejiang Kangle Pharmaceutical Co., Ltd (Binhai Plant)

Zhejiang Kangle Pharmaceutical Co., Ltd (Binhai Plant) — FEI 3010728912

The FDA completed an inspection of Zhejiang Kangle Pharmaceutical Co., Ltd (Binhai Plant) on Mar 14, 2025 in Wenzhou. 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
Mar 14, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wenzhou (China)

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