Aurora Importing & Distributing Ltd
⚠️ Moderate Risk
FEI: 3004290694 • Mississauga, Ontario • CANADA
FEI Number
3004290694
Location
Mississauga, Ontario
Country
CANADAAddress
815 Gana Crt, , Mississauga, Ontario, Canada
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
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.
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
PRESRV LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/22/2017 | 24FCI01EGG PLANT (FRUIT USED AS VEGETABLE) | New York District Office (NYK-DO) | |
| 2/12/2002 | 03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | 482NUTRIT LBL | New York District Office (NYK-DO) |
| 2/12/2002 | 33EGT14TAFFY (TOFFEE), KISSES CANDY, HARD, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | 482NUTRIT LBL | New York District Office (NYK-DO) |
| 2/12/2002 | 03CGT09NON-STANDARD BREADS, ROLLS, BUNS, ETC PREPARED DRY MIX WITHOUT MILK OR EGG | 482NUTRIT LBL | New York District Office (NYK-DO) |
| 2/12/2002 | 33EGT14TAFFY (TOFFEE), KISSES CANDY, HARD, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | 482NUTRIT LBL | New York District Office (NYK-DO) |
| 2/12/2002 | 03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | 482NUTRIT LBL | New York District Office (NYK-DO) |
| 2/12/2002 | 27YCT04HORSERADISH, PREPARED | New York District Office (NYK-DO) | |
| 2/12/2002 | 23EYY06FILBERT, HAZELNUT, SPREAD | New York District Office (NYK-DO) | |
| 1/8/2002 | 25HCI99MIXED VEGETABLES, WITH SAUCE, N.E.C. | New York District Office (NYK-DO) | |
| 1/8/2002 | 24AEE11PINTO BEAN | 62NEEDS FCE | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Aurora Importing & Distributing Ltd's FDA import refusal history?
Aurora Importing & Distributing Ltd (FEI: 3004290694) has 10 FDA import refusal record(s) in our database, spanning from 1/8/2002 to 2/22/2017.
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. Aurora Importing & Distributing Ltd's FEI number is 3004290694.
What types of violations has Aurora Importing & Distributing Ltd received?
Aurora Importing & Distributing Ltd 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 Aurora Importing & Distributing Ltd come from?
All FDA import refusal data for Aurora Importing & Distributing Ltd 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.