Jim Faulkner Associates
⚠️ Moderate Risk
FEI: 3003508543 • Brampton, ON • CANADA
FEI Number
3003508543
Location
Brampton, ON
Country
CANADAAddress
23 Kenpark Ave, , Brampton, ON, 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.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/29/2003 | 41AGT99FOODS WITH ARTIFICIAL SWEETNERS BUT WITHOUT SUPPLEMENTAL NUTRIENTS | New York District Office (NYK-DO) | |
| 10/29/2003 | 29BGT50SOFT DRINK, COLA, CARBONATED | New York District Office (NYK-DO) | |
| 10/29/2003 | 29BGT02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED | New York District Office (NYK-DO) | |
| 10/7/2003 | 29BGT50SOFT DRINK, COLA, CARBONATED | New York District Office (NYK-DO) | |
| 10/7/2003 | 29BGT50SOFT DRINK, COLA, CARBONATED | New York District Office (NYK-DO) | |
| 10/7/2003 | 29BGT02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Jim Faulkner Associates's FDA import refusal history?
Jim Faulkner Associates (FEI: 3003508543) has 6 FDA import refusal record(s) in our database, spanning from 10/7/2003 to 10/29/2003.
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. Jim Faulkner Associates's FEI number is 3003508543.
What types of violations has Jim Faulkner Associates received?
Jim Faulkner Associates 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 Jim Faulkner Associates come from?
All FDA import refusal data for Jim Faulkner Associates 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.