Sosagrin
⚠️ Moderate Risk
FEI: 2000006724 • Dakar • SENEGAL
FEI Number
2000006724
Location
Dakar
Country
SENEGALAddress
Rue N6 Km 4,5 Bd Du Centenaire De La, Commune De Dakar, Dakar, , Senegal
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.
SULFITELBL
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because 1) it appears to contain sulfites but the label fails to declare the presence of sulfites, a fact material to sulfite-sensitive individuals who must avoid the ingredient due to potential health consequences from its consumption, and 2) it appears the food is fabricated from two or more ingredients and the label does not list the common or usual name of each ingredient.
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/5/2015 | 27YGT05MUSTARD, PREPARED | Seattle District Office (SEA-DO) | |
| 10/5/2015 | 27YGT05MUSTARD, PREPARED | Seattle District Office (SEA-DO) | |
| 3/12/2010 | 27YEY05MUSTARD, PREPARED | 482NUTRIT LBL | New York District Office (NYK-DO) |
| 3/12/2010 | 27YCY05MUSTARD, PREPARED | 482NUTRIT LBL | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Sosagrin's FDA import refusal history?
Sosagrin (FEI: 2000006724) has 4 FDA import refusal record(s) in our database, spanning from 3/12/2010 to 10/5/2015.
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. Sosagrin's FEI number is 2000006724.
What types of violations has Sosagrin received?
Sosagrin 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 Sosagrin come from?
All FDA import refusal data for Sosagrin 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.