FDA Inspection 1091073 — Hans Biomed Corporation

Hans Biomed Corporation — FEI 3003828812

The FDA completed an inspection of Hans Biomed Corporation on Apr 5, 2019 in Yuseong District. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 5, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Yuseong District (Korea (the Republic of))

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