VINH QUANG FISHERIES CORP.
⚠️ High Risk
FEI: 2000009471 • My Tho, Tien Giang • VIETNAM
FEI Number
2000009471
Location
My Tho, Tien Giang
Country
VIETNAMAddress
Lot 37-40, My Tho Industrial Park, , My Tho, Tien Giang, Vietnam
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
Frequently Asked Questions
What is VINH QUANG FISHERIES CORP.'s FDA import refusal history?
VINH QUANG FISHERIES CORP. (FEI: 2000009471) has 3 FDA import refusal record(s) in our database, spanning from 7/6/2022 to 7/6/2022.
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. VINH QUANG FISHERIES CORP.'s FEI number is 2000009471.
What types of violations has VINH QUANG FISHERIES CORP. received?
VINH QUANG FISHERIES CORP. 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 VINH QUANG FISHERIES CORP. come from?
All FDA import refusal data for VINH QUANG FISHERIES CORP. 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.