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FDA Inspection 848720 — Hans Biomed Corporation

Hans Biomed Corporation — FEI 3003828812

The FDA completed an inspection of Hans Biomed Corporation on August 29, 2013 in Yuseong District. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 29, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Yuseong District (Korea (the Republic of))

Facility

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