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JGB S.A.

⚠️ Moderate Risk

FEI: 3011367081 • Cali, Valle Del Cauca • COLOMBIA

FEI

FEI Number

3011367081

📍

Location

Cali, Valle Del Cauca

🇨🇴

Country

COLOMBIA
🏢

Address

Carrera 5 23 82, , Cali, Valle Del Cauca, Colombia

Moderate Risk

FDA Import Risk Assessment

25.4
LowModerateHighCritical

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

Statistics

5
Total Refusals
7
Unique Violations
8/7/2014
Latest Refusal
9/1/2004
Earliest Refusal

Score Breakdown

Violation Severity
40.7×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
5.0×10%
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

4823×

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.

2183×

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.

3412×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32802×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

2561×

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)).

23001×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

Refusal History

DateProductViolationsDivision
8/7/2014
76JESFLOSS, DENTAL
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Florida District Office (FLA-DO)
8/7/2014
76EFWTOOTHBRUSH, MANUAL
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Florida District Office (FLA-DO)
1/28/2014
54YCZ99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
482NUTRIT LBL
Florida District Office (FLA-DO)
10/31/2013
54YCZ99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
482NUTRIT LBL
Florida District Office (FLA-DO)
9/1/2004
54AER01VITAMIN A
218LIST INGRE
2300DIETARYLBL
256INCONSPICU
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is JGB S.A.'s FDA import refusal history?

JGB S.A. (FEI: 3011367081) has 5 FDA import refusal record(s) in our database, spanning from 9/1/2004 to 8/7/2014.

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. JGB S.A.'s FEI number is 3011367081.

What types of violations has JGB S.A. received?

JGB S.A. has been cited for 7 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 JGB S.A. come from?

All FDA import refusal data for JGB S.A. 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.