FDA Inspection 853887 — ALPHANOX CO., LTD.

ALPHANOX CO., LTD. — FEI 3004941535

The FDA completed an inspection of ALPHANOX CO., LTD. on September 12, 2013 in Pyeongtaek. 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
September 12, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Pyeongtaek (Korea (the Republic of))