Hong Lien
⚠️ Moderate Risk
FEI: 3007912500 • Binh Thanh Ho Chi Ming • VIETNAM
FEI Number
3007912500
Location
Binh Thanh Ho Chi Ming
Country
VIETNAMAddress
146/14/13 Vu Tung Street Ward 2, , Binh Thanh Ho Chi Ming, , Vietnam
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
OFF ODOR
The article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food. Contains an off odor.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/13/2010 | 16AGT99FISH, N.E.C. | 337OFF ODOR | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Hong Lien's FDA import refusal history?
Hong Lien (FEI: 3007912500) has 1 FDA import refusal record(s) in our database, spanning from 10/13/2010 to 10/13/2010.
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. Hong Lien's FEI number is 3007912500.
What types of violations has Hong Lien received?
Hong Lien 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 Hong Lien come from?
All FDA import refusal data for Hong Lien 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.