DULCERIA AURORA
⚠️ Moderate Risk
FEI: 3020834735 • Cofradia, Cortes • HONDURAS
FEI Number
3020834735
Location
Cofradia, Cortes
Country
HONDURASAddress
Barrio El Cacao, , Cofradia, Cortes, Honduras
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
INSANITARY
The article is subject to refusal of admission pursuant to section 801(a)(3) in that the article appears to have been prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth, or whereby it may have been rendered injurious to health.
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.
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.
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.
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.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/5/2022 | 33JHT06FLAVORED CANDY, SOFT (LIVE SAVERS, ETC.), WITH FRUIT (WITHOUT CHOCOLATE) | Division of Southwest Imports (DSWI) | |
| 8/5/2022 | 21UHB48COCONUT, SUBTROPICAL AND TROPICAL FRUIT, JAMS, JELLIES, PRESERVES, MARMALADES, CANDIED, BUTTERS, SPR | Division of Southwest Imports (DSWI) | |
| 7/18/2022 | 21JGT14PLUM, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | 186INSANITARY | Division of Southwest Imports (DSWI) |
| 7/18/2022 | 23BGT03CASHEW, SHELLED | 186INSANITARY | Division of Southwest Imports (DSWI) |
| 7/18/2022 | 33JHT06FLAVORED CANDY, SOFT (LIVE SAVERS, ETC.), WITH FRUIT (WITHOUT CHOCOLATE) | 186INSANITARY | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is DULCERIA AURORA's FDA import refusal history?
DULCERIA AURORA (FEI: 3020834735) has 5 FDA import refusal record(s) in our database, spanning from 7/18/2022 to 8/5/2022.
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. DULCERIA AURORA's FEI number is 3020834735.
What types of violations has DULCERIA AURORA received?
DULCERIA AURORA has been cited for 7 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 DULCERIA AURORA come from?
All FDA import refusal data for DULCERIA AURORA 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.