NESTLE DE COLOMBIA
⚠️ Moderate Risk
FEI: 3013350983 • Bogota, Distrito Capital de Bogota • COLOMBIA
FEI Number
3013350983
Location
Bogota, Distrito Capital de Bogota
Country
COLOMBIAAddress
18 No 96 41, , Bogota, Distrito Capital de Bogota, 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.
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.
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).
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.
TRANSFAT
The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].
INCONSPICU
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)).
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).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/25/2019 | 03JGT07MIXED FILLED/ICED COOKIES,BISCUITS AND WAFERS | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 6/1/2015 | 03MGT99COOKIE,BISCUIT,WAFER DOUGH, N.E.C. | Florida District Office (FLA-DO) | |
| 6/1/2015 | 03MGT99COOKIE,BISCUIT,WAFER DOUGH, N.E.C. | Florida District Office (FLA-DO) | |
| 6/25/2014 | 03AGT03BISCUITS | 482NUTRIT LBL | Florida District Office (FLA-DO) |
| 6/25/2014 | 34FHN07MIXED OR ASSORTED CHOCOLATE CANDIES (BARS, BOXES, LOOSE FORM), WITHOUT NUTS AND FRUIT | Florida District Office (FLA-DO) | |
| 6/25/2014 | 03AGT03BISCUITS | 324NO ENGLISH | Florida District Office (FLA-DO) |
| 3/26/2013 | 03RGT01CAKE WITHOUT CUSTARD OR CREAM FILLING | Florida District Office (FLA-DO) | |
| 3/26/2013 | 03RGT01CAKE WITHOUT CUSTARD OR CREAM FILLING | Florida District Office (FLA-DO) | |
| 9/13/2012 | 03RGT01CAKE WITHOUT CUSTARD OR CREAM FILLING | Florida District Office (FLA-DO) | |
| 9/13/2012 | 03MGT99COOKIE,BISCUIT,WAFER DOUGH, N.E.C. | 324NO ENGLISH | Florida District Office (FLA-DO) |
| 9/13/2012 | 03RGT01CAKE WITHOUT CUSTARD OR CREAM FILLING | 11UNSAFE COL | Florida District Office (FLA-DO) |
| 11/16/2010 | 03HMT10CREME,PLAIN COOKIE, BISCUIT AND WAFER | New York District Office (NYK-DO) | |
| 11/16/2010 | 03HMT10CREME,PLAIN COOKIE, BISCUIT AND WAFER | New York District Office (NYK-DO) | |
| 11/16/2010 | 03HMT10CREME,PLAIN COOKIE, BISCUIT AND WAFER | New York District Office (NYK-DO) | |
| 10/16/2006 | 28BHT99SPICES, GROUND, CRACKED, ETC., N.E.C. | Florida District Office (FLA-DO) | |
| 9/29/2006 | 38ADT99SOUP, N.E.C. | Florida District Office (FLA-DO) | |
| 8/31/2004 | 09CET03MILK, CONCENTRATED, EVAPORATED AND CONDENSED | Florida District Office (FLA-DO) | |
| 8/31/2004 | 09CET03MILK, CONCENTRATED, EVAPORATED AND CONDENSED | Florida District Office (FLA-DO) | |
| 3/20/2003 | 09CEE03MILK, CONCENTRATED, EVAPORATED AND CONDENSED | Florida District Office (FLA-DO) | |
| 12/10/2002 | 09CEE03MILK, CONCENTRATED, EVAPORATED AND CONDENSED | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is NESTLE DE COLOMBIA's FDA import refusal history?
NESTLE DE COLOMBIA (FEI: 3013350983) has 20 FDA import refusal record(s) in our database, spanning from 12/10/2002 to 4/25/2019.
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. NESTLE DE COLOMBIA's FEI number is 3013350983.
What types of violations has NESTLE DE COLOMBIA received?
NESTLE DE COLOMBIA has been cited for 9 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 NESTLE DE COLOMBIA come from?
All FDA import refusal data for NESTLE DE COLOMBIA 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.