LIDERPAN SA EN REORGANIZACION
⚠️ Moderate Risk
FEI: 3011418221 • Yumbo, Valle del Cauca • COLOMBIA
FEI Number
3011418221
Location
Yumbo, Valle del Cauca
Country
COLOMBIAAddress
Carrera 12 14a 140, , Yumbo, Valle del Cauca, Colombia
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
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)).
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.
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.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/31/2024 | 03AGT03BISCUITS | Division of Southeast Imports (DSEI) | |
| 1/5/2022 | 03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 8/1/2018 | 03MYY99COOKIE,BISCUIT,WAFER DOUGH, N.E.C. | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 10/25/2017 | 03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | 482NUTRIT LBL | Division of Northeast Imports (DNEI) |
| 5/31/2017 | 03MGT99COOKIE,BISCUIT,WAFER DOUGH, N.E.C. | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is LIDERPAN SA EN REORGANIZACION's FDA import refusal history?
LIDERPAN SA EN REORGANIZACION (FEI: 3011418221) has 5 FDA import refusal record(s) in our database, spanning from 5/31/2017 to 5/31/2024.
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. LIDERPAN SA EN REORGANIZACION's FEI number is 3011418221.
What types of violations has LIDERPAN SA EN REORGANIZACION received?
LIDERPAN SA EN REORGANIZACION 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 LIDERPAN SA EN REORGANIZACION come from?
All FDA import refusal data for LIDERPAN SA EN REORGANIZACION 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.