Zee-Teck
⚠️ High Risk
FEI: 3020109351 • Abuja, Abuja Federal Capital Territor • NIGERIA
FEI Number
3020109351
Location
Abuja, Abuja Federal Capital Territor
Country
NIGERIAAddress
12 Biliri Street, Garki 2, , Abuja, Abuja Federal Capital Territor, Nigeria
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable 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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/6/2024 | 02HHT01TAPIOCA STARCH PRODUCT | 249FILTHY | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is Zee-Teck's FDA import refusal history?
Zee-Teck (FEI: 3020109351) has 1 FDA import refusal record(s) in our database, spanning from 5/6/2024 to 5/6/2024.
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. Zee-Teck's FEI number is 3020109351.
What types of violations has Zee-Teck received?
Zee-Teck 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 Zee-Teck come from?
All FDA import refusal data for Zee-Teck 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.