FDA Inspection 1275219 — Broadleaf USA Inc.

Broadleaf USA Inc. — FEI 3003478405

The FDA completed an inspection of Broadleaf USA Inc. on Jul 7, 2025 in Vernon, CA. 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
Jul 7, 2025
Fiscal Year
2025
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Vernon, CA (United States)

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