FDA Inspection 853887 — ALPHANOX CO., LTD.

ALPHANOX CO., LTD. — FEI 3004941535

The FDA completed an inspection of ALPHANOX CO., LTD. on Sep 12, 2013 in Pyeongtaek. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Sep 12, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Pyeongtaek (Korea (the Republic of))

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