FDA Inspection 1256783 — Zhejiang Poly Pharm. Co., Ltd

Zhejiang Poly Pharm. Co., Ltd — FEI 3014405699

The FDA completed an inspection of Zhejiang Poly Pharm. Co., Ltd on Nov 8, 2024 in Hangzhou. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 8, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hangzhou (China)

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