FDA Inspection 1300242 — Hebei Meishen Technology Co., Ltd.

Hebei Meishen Technology Co., Ltd. — FEI 3014541740

The FDA completed an inspection of Hebei Meishen Technology Co., Ltd. on Dec 18, 2025 in Xingtai. 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
Dec 18, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Xingtai (China)

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