FDA Inspection 1281282 — GREENLEAF
The FDA completed an inspection of GREENLEAF on Sep 11, 2025 in Lisle, IL. 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 11, 2025
- Fiscal Year
- 2025
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Lisle, IL (United States)
Additional Details
FSVP