FDA Inspection 1280826 — Boortmalt USA Limited

Boortmalt USA Limited — FEI 2120764

The FDA completed an inspection of Boortmalt USA Limited on Aug 14, 2025 in Sheboygan, WI. 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 14, 2025
Fiscal Year
2025
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Sheboygan, WI (United States)

Additional Details

FSVP

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