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FDA Inspection 802448 — I-Sens Wonju Factory

I-Sens Wonju Factory — FEI 3007382160

The FDA completed an inspection of I-Sens Wonju Factory on Sep 11, 2012 in Wonju. 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 11, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Wonju (Korea (the Republic of))

Facility

FDA data resources

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