FDA Inspection 1341510 — InjeOmija Manufacturing

InjeOmija Manufacturing — FEI 3015045182

The FDA completed an inspection of InjeOmija Manufacturing on Sep 15, 2026 in Inje. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 15, 2026
Fiscal Year
2026
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Inje (Korea (the Republic of))

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