La Sopra
⚠️ Moderate Risk
FEI: 3011714962 • Dakar • SENEGAL
FEI Number
3011714962
Location
Dakar
Country
SENEGALAddress
35 Cite Dalifort Villa, , 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
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.
NO ENGLISH
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/20/2015 | 24FCI08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | Division of Northeast Imports (DNEI) | |
| 10/20/2015 | 24FCI08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | Division of Northeast Imports (DNEI) | |
| 10/5/2015 | 27YCT06PEPPER SAUCE (HOT, MILD, ETC.) | Seattle District Office (SEA-DO) | |
| 10/5/2015 | 27YGT06PEPPER SAUCE (HOT, MILD, ETC.) | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is La Sopra's FDA import refusal history?
La Sopra (FEI: 3011714962) has 4 FDA import refusal record(s) in our database, spanning from 10/5/2015 to 10/20/2015.
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. La Sopra's FEI number is 3011714962.
What types of violations has La Sopra received?
La Sopra 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 La Sopra come from?
All FDA import refusal data for La Sopra 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.