FDA Inspection 1301468 — Fujian Genohope Biotech Ltd

Fujian Genohope Biotech Ltd — FEI 3025263427

The FDA completed an inspection of Fujian Genohope Biotech Ltd on Jan 16, 2026 in Futian. 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
Jan 16, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Futian (China)

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