Huong Que Manufacturer
⚠️ Moderate Risk
FEI: 2000033941 • Ho Chi Minh City, VN-65 • VIETNAM
FEI Number
2000033941
Location
Ho Chi Minh City, VN-65
Country
VIETNAMAddress
C29/148 Ni Su Huynh Lien, P. 10, Q. Tan Binh, Ho Chi Minh City, VN-65, 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
LACKS N/C
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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
SULFITELBL
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because 1) it appears to contain sulfites but the label fails to declare the presence of sulfites, a fact material to sulfite-sensitive individuals who must avoid the ingredient due to potential health consequences from its consumption, and 2) it appears the food is fabricated from two or more ingredients and the label does not list the common or usual name of each ingredient.
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.
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)).
YELLOW #5
The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/12/2008 | 21UYY05MANGO, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | Southwest Import District Office (SWI-DO) | |
| 10/29/2007 | 21JYY15PRUNES (DRIED PLUMS), JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | Southwest Import District Office (SWI-DO) | |
| 10/29/2007 | 21JYY13PEACH, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | Southwest Import District Office (SWI-DO) | |
| 10/29/2007 | 21JYY03CHERRY, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Huong Que Manufacturer's FDA import refusal history?
Huong Que Manufacturer (FEI: 2000033941) has 4 FDA import refusal record(s) in our database, spanning from 10/29/2007 to 2/12/2008.
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. Huong Que Manufacturer's FEI number is 2000033941.
What types of violations has Huong Que Manufacturer received?
Huong Que Manufacturer has been cited for 6 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 Huong Que Manufacturer come from?
All FDA import refusal data for Huong Que Manufacturer 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.