FDA Inspection 1303124 — Boortmalt USA Limited
The FDA completed an inspection of Boortmalt USA Limited on February 9, 2026 in Sheboygan, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 9, 2026
- Fiscal Year
- 2026
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Sheboygan, WI (United States)