FDA Inspection 1283018 — Koninklijke Euroma B.V.

Koninklijke Euroma B.V. — FEI 3004347849

The FDA completed an inspection of Koninklijke Euroma B.V. on Aug 12, 2025 in Zwolle. 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
Aug 12, 2025
Fiscal Year
2025
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Zwolle (Netherlands)

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