CORE FULFILMENT
✅ Low Risk
FEI: 3013423357 • Sandbach • UNITED KINGDOM
FEI Number
3013423357
Location
Sandbach
Country
UNITED KINGDOMAddress
Lodge Road, , Sandbach, , United Kingdom
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/8/2017 | 54YCA99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 473LABELING | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is CORE FULFILMENT's FDA import refusal history?
CORE FULFILMENT (FEI: 3013423357) has 1 FDA import refusal record(s) in our database, spanning from 6/8/2017 to 6/8/2017.
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. CORE FULFILMENT's FEI number is 3013423357.
What types of violations has CORE FULFILMENT received?
CORE FULFILMENT has been cited for 1 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 CORE FULFILMENT come from?
All FDA import refusal data for CORE FULFILMENT 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.