hacota
⚠️ Moderate Risk
FEI: 3005039208 • silver spring, VN-65 • VIETNAM
FEI Number
3005039208
Location
silver spring, VN-65
Country
VIETNAMAddress
8 nguyen binh khiem str, dist.1, hcmc, , silver spring, 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.
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
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.
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.
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/6/2005 | 16CGT82FRESHWATER NON-ICTALURUS FISH, CAKES, BALLS, ETC. | Los Angeles District Office (LOS-DO) | |
| 6/6/2005 | 16AHP73MACKEREL (ALL EXCEPT SCOMBEROMORUS SP, EG SPANISH OR KING SEE '22') | Los Angeles District Office (LOS-DO) | |
| 6/6/2005 | 16AGP99FISH, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 5/6/2004 | 23BGT14BETEL NUT, SHELLED | 251POISONOUS | Los Angeles District Office (LOS-DO) |
| 7/30/2003 | 16MGF09OCTOPUS, OTHER AQUATIC SPECIES | Los Angeles District Office (LOS-DO) | |
| 7/30/2003 | 16AGF99FISH, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 7/30/2003 | 16AGF73MACKEREL (ALL EXCEPT SCOMBEROMORUS SP, EG SPANISH OR KING SEE '22') | Los Angeles District Office (LOS-DO) | |
| 6/2/2003 | 16AGF99FISH, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 6/2/2003 | 16AGF23MULLET | Los Angeles District Office (LOS-DO) | |
| 6/2/2003 | 16AGF99FISH, N.E.C. | 9SALMONELLA | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is hacota's FDA import refusal history?
hacota (FEI: 3005039208) has 10 FDA import refusal record(s) in our database, spanning from 6/2/2003 to 6/6/2005.
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. hacota's FEI number is 3005039208.
What types of violations has hacota received?
hacota has been cited for 8 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 hacota come from?
All FDA import refusal data for hacota 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.