BEN THANH MARKET
⚠️ Moderate Risk
FEI: 3013057812 • Ho Chi Minh • VIETNAM
FEI Number
3013057812
Location
Ho Chi Minh
Country
VIETNAMAddress
36, 30, Phan Boi Chau St, Ho Chi Minh, , 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
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)).
MFRHACCP
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Act in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health in that it appears to have been processed in violation of 21 CFR 123.6(a) and 123.8(a).
FOREIGN OB
The article appears to consist in whole or in part of a filthy, putrid, or decomposed substance, or is otherwise unfit for food in that it appears to contain foreign objects.
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.
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/12/2017 | 16AYY99FISH, N.E.C. | Division of Southeast Imports (DSEI) | |
| 1/12/2017 | 16MYH03SQUID, OTHER AQUATIC SPECIES | Division of Southeast Imports (DSEI) | |
| 1/12/2017 | 28AYH54PEPPER,BLACK, WHOLE (SPICE) | Division of Southeast Imports (DSEI) | |
| 1/12/2017 | 28JYT99MIXED SPICES AND SEASONING WITH SALT, N.E.C. | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is BEN THANH MARKET's FDA import refusal history?
BEN THANH MARKET (FEI: 3013057812) has 4 FDA import refusal record(s) in our database, spanning from 1/12/2017 to 1/12/2017.
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. BEN THANH MARKET's FEI number is 3013057812.
What types of violations has BEN THANH MARKET received?
BEN THANH MARKET 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 BEN THANH MARKET come from?
All FDA import refusal data for BEN THANH MARKET 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.