Fruition Fruits & Fills
⚠️ Moderate Risk
FEI: 3004352022 • Oakville, Ontario • CANADA
FEI Number
3004352022
Location
Oakville, Ontario
Country
CANADAAddress
2379 Speers Rd, , Oakville, 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
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.
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).
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.
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 |
|---|---|---|---|
| 4/3/2013 | 21CHT99MIXED FRUIT, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED, N.E.C. | New York District Office (NYK-DO) | |
| 4/3/2013 | 03YET99OTHER BAKERY PRODUCTS, N.E.C. | New York District Office (NYK-DO) | |
| 11/10/2009 | 21JHT13PEACH, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | 218LIST INGRE | New York District Office (NYK-DO) |
| 11/10/2009 | 21JHT13PEACH, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | 218LIST INGRE | New York District Office (NYK-DO) |
| 11/10/2009 | 21JHT13PEACH, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | 218LIST INGRE | New York District Office (NYK-DO) |
| 8/27/2009 | 20CHT13RASPBERRY, RED, JAM, JELLY, PRESERVES, MARMALADE, BUTTER AND CANDIED | 306INSANITARY | New York District Office (NYK-DO) |
| 8/27/2009 | 21JHT13PEACH, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | 218LIST INGRE | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Fruition Fruits & Fills's FDA import refusal history?
Fruition Fruits & Fills (FEI: 3004352022) has 7 FDA import refusal record(s) in our database, spanning from 8/27/2009 to 4/3/2013.
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. Fruition Fruits & Fills's FEI number is 3004352022.
What types of violations has Fruition Fruits & Fills received?
Fruition Fruits & Fills has been cited for 4 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 Fruition Fruits & Fills come from?
All FDA import refusal data for Fruition Fruits & Fills 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.