Huynh Vu
⚠️ Moderate Risk
FEI: 3008339118 • Ho Chi Minh City • VIETNAM
FEI Number
3008339118
Location
Ho Chi Minh City
Country
VIETNAMAddress
No 27/40/158 Huynh Tinh Cua Strward 8, , Ho Chi Minh City, , 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
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.
LACKS FIRM
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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
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.
USUAL NAME
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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/22/2010 | 28AGH99WHOLE SPICE, N.E.C. | Minneapolis District Office (MIN-DO) | |
| 7/22/2010 | 28AGT13CINNAMON, CASSIA, WHOLE (SPICE) | Minneapolis District Office (MIN-DO) | |
| 7/22/2010 | 02HYY99STARCH PRODUCTS N.E.C. | Minneapolis District Office (MIN-DO) | |
| 7/22/2010 | 31KGY99TEA, N.E.C. | Minneapolis District Office (MIN-DO) | |
| 7/22/2010 | 28YYY99SPICES, FLAVORS AND SALT NOT MENTIONED ELSEWHERE, N.E.C. | Minneapolis District Office (MIN-DO) | |
| 7/22/2010 | 35AGT03AGAR AGAR (GELATIN PRODUCT) | Minneapolis District Office (MIN-DO) |
Frequently Asked Questions
What is Huynh Vu's FDA import refusal history?
Huynh Vu (FEI: 3008339118) has 6 FDA import refusal record(s) in our database, spanning from 7/22/2010 to 7/22/2010.
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. Huynh Vu's FEI number is 3008339118.
What types of violations has Huynh Vu received?
Huynh Vu has been cited for 5 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 Huynh Vu come from?
All FDA import refusal data for Huynh Vu 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.