NGHI TUYET DUONG
⚠️ Moderate Risk
FEI: 3015843781 • Quan Tan Phu • VIETNAM
FEI Number
3015843781
Location
Quan Tan Phu
Country
VIETNAMAddress
19, 106, Duong Hoa Binh, Quan Tan Phu, , 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
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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.
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
NO ENGLISH
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/1/2019 | 25JHT25ONION BULB (YELLOW, WHITE, RED, ETC.) (ROOT & TUBER VEGETABLE) | Division of West Coast Imports (DWCI) | |
| 11/1/2019 | 21GGY14PLUM (PIT FRUIT) | Division of West Coast Imports (DWCI) | |
| 11/1/2019 | 25JHT21GARLIC BULB (ROOT & TUBER VEGETABLE) | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is NGHI TUYET DUONG's FDA import refusal history?
NGHI TUYET DUONG (FEI: 3015843781) has 3 FDA import refusal record(s) in our database, spanning from 11/1/2019 to 11/1/2019.
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. NGHI TUYET DUONG's FEI number is 3015843781.
What types of violations has NGHI TUYET DUONG received?
NGHI TUYET DUONG has been cited for 4 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 NGHI TUYET DUONG come from?
All FDA import refusal data for NGHI TUYET DUONG 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.