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FRITO LAY COLOMBIA LTD

⚠️ Moderate Risk

FEI: 3005971712 • Bogota, Distrito Capital de Bogota • COLOMBIA

FEI

FEI Number

3005971712

📍

Location

Bogota, Distrito Capital de Bogota

🇨🇴

Country

COLOMBIA
🏢

Address

Calle 90 # 21-74, , Bogota, Distrito Capital de Bogota, Colombia

Moderate Risk

FDA Import Risk Assessment

27.0
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

9
Total Refusals
8
Unique Violations
7/24/2013
Latest Refusal
2/15/2007
Earliest Refusal

Score Breakdown

Violation Severity
36.3×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
14.0×10%
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

3249×

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)).

3201×

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.

3211×

LACKS N/C

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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

3281×

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.

33001×

ALLERGEN

the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

2181×

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.

4821×

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.

Refusal History

DateProductViolationsDivision
7/24/2013
07BGT02CORN CHIPS, FRIED
324NO ENGLISH
Florida District Office (FLA-DO)
4/25/2011
23BGT07PEANUT, SHELLED
218LIST INGRE
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
328USUAL NAME
3300ALLERGEN
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
5/11/2010
07AGT03CHEESE PUFFS, BAKED
324NO ENGLISH
Division of Southeast Imports (DSEI)
5/11/2010
07AGT99BAKED SNACK FOOD, N.E.C.
324NO ENGLISH
Division of Southeast Imports (DSEI)
2/15/2007
33ADT99HARD CANDY WITH NUT OR NUT PRODUCTS, N.E.C. (WITHOUT CHOCOLATE)
324NO ENGLISH
Division of Southeast Imports (DSEI)
2/15/2007
07ADT02CORN CHIPS, BAKED
324NO ENGLISH
Division of Southeast Imports (DSEI)
2/15/2007
07BDT06POTATO CHIPS,FRIED
324NO ENGLISH
Division of Southeast Imports (DSEI)
2/15/2007
07ADT06POTATO CHIPS,BAKED
324NO ENGLISH
Division of Southeast Imports (DSEI)
2/15/2007
34FGT04CHOCOLATE COVERED CANDY PIECES, WITHOUT NUTS AND FRUIT
324NO ENGLISH
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is FRITO LAY COLOMBIA LTD's FDA import refusal history?

FRITO LAY COLOMBIA LTD (FEI: 3005971712) has 9 FDA import refusal record(s) in our database, spanning from 2/15/2007 to 7/24/2013.

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. FRITO LAY COLOMBIA LTD's FEI number is 3005971712.

What types of violations has FRITO LAY COLOMBIA LTD received?

FRITO LAY COLOMBIA LTD has been cited for 8 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 FRITO LAY COLOMBIA LTD come from?

All FDA import refusal data for FRITO LAY COLOMBIA LTD 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.