Socodal
⚠️ Moderate Risk
FEI: 3014405937 • Dar Allouche, Nabeul • TUNISIA
FEI Number
3014405937
Location
Dar Allouche, Nabeul
Country
TUNISIAAddress
111 Boulevard Environnement, , Dar Allouche, Nabeul, Tunisia
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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.
LACKS FIRM
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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
USUAL NAME
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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
FSVP VIO
The article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) in that it appears that the importer (as defined in section 805 of the FD&C Act) is in violation of section 805.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/24/2022 | 27YET06PEPPER SAUCE (HOT, MILD, ETC.) | 3886FSVP VIO | Division of Northern Border Imports (DNBI) |
| 6/27/2018 | 27YET06PEPPER SAUCE (HOT, MILD, ETC.) | Division of Northern Border Imports (DNBI) | |
| 6/27/2018 | 27YET06PEPPER SAUCE (HOT, MILD, ETC.) | Division of Northern Border Imports (DNBI) | |
| 6/27/2018 | 27YEI06PEPPER SAUCE (HOT, MILD, ETC.) | Division of Northern Border Imports (DNBI) | |
| 6/27/2018 | 27YEI06PEPPER SAUCE (HOT, MILD, ETC.) | Division of Northern Border Imports (DNBI) | |
| 9/24/2013 | 27YEB02CHILE PUREE | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Socodal's FDA import refusal history?
Socodal (FEI: 3014405937) has 6 FDA import refusal record(s) in our database, spanning from 9/24/2013 to 2/24/2022.
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. Socodal's FEI number is 3014405937.
What types of violations has Socodal received?
Socodal 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 Socodal come from?
All FDA import refusal data for Socodal 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.