FDA Inspection 1303124 — Boortmalt USA Limited

Boortmalt USA Limited — FEI 2120764

The FDA completed an inspection of Boortmalt USA Limited on Feb 9, 2026 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
Feb 9, 2026
Fiscal Year
2026
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Sheboygan, WI (United States)

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