Fonterra Limited
⚠️ Moderate Risk
FEI: 3012336777 • Auckland • NEW ZEALAND
FEI Number
3012336777
Location
Auckland
Country
NEW ZEALANDAddress
109 Fanshawe Street, , Auckland, , New Zealand
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
HEALTH C
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling bears an unauthorized nutrient content/health claim.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/17/2021 | 09CEH16MILK, DRIED | Division of Northeast Imports (DNEI) | |
| 2/17/2021 | 09CEH16MILK, DRIED | Division of Northeast Imports (DNEI) | |
| 2/17/2021 | 09CEH16MILK, DRIED | Division of Northeast Imports (DNEI) | |
| 2/17/2021 | 09CEH16MILK, DRIED | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Fonterra Limited's FDA import refusal history?
Fonterra Limited (FEI: 3012336777) has 4 FDA import refusal record(s) in our database, spanning from 2/17/2021 to 2/17/2021.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Fonterra Limited's FEI number is 3012336777.
What types of violations has Fonterra Limited received?
Fonterra Limited has been cited for 2 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Fonterra Limited come from?
All FDA import refusal data for Fonterra Limited is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.