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C. I. Vega & Vega Ltda.

⚠️ Moderate Risk

FEI: 3003400099 • Medellin • COLOMBIA

FEI

FEI Number

3003400099

📍

Location

Medellin

🇨🇴

Country

COLOMBIA
🏢

Address

Calle 15 Sur No. 46-120, , Medellin, , Colombia

Moderate Risk

FDA Import Risk Assessment

40.6
LowModerateHighCritical

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

Statistics

13
Total Refusals
5
Unique Violations
10/30/2002
Latest Refusal
10/3/2001
Earliest Refusal

Score Breakdown

Violation Severity
44.7×40%
Refusal Volume
42.5×30%
Recency
0.0×20%
Frequency
100.0×10%
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

4827×

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.

2746×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

2182×

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.

621×

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).

831×

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.

Refusal History

DateProductViolationsDivision
10/30/2002
29BEY60SODA WATER, CARBONATED
274COLOR LBLG
San Juan District Office (SJN-DO)
2/28/2002
23BEY07PEANUT, SHELLED
482NUTRIT LBL
San Juan District Office (SJN-DO)
2/28/2002
38AEN23POTATO SOUP
482NUTRIT LBL
San Juan District Office (SJN-DO)
2/28/2002
29BCT09SOFT DRINK, OTHER FRUIT FLAVORED, CARBONATED
482NUTRIT LBL
San Juan District Office (SJN-DO)
2/28/2002
24AGT99BEANS, CORN, AND PEA, N.E.C. (VEGETABLE)
482NUTRIT LBL
San Juan District Office (SJN-DO)
2/28/2002
21TWT04GUAVA, DRIED OR PASTE
274COLOR LBLG
482NUTRIT LBL
San Juan District Office (SJN-DO)
2/28/2002
29BGT99CARBONATED SOFT DRINK, N.E.C.
274COLOR LBLG
San Juan District Office (SJN-DO)
2/28/2002
29BGT99CARBONATED SOFT DRINK, N.E.C.
274COLOR LBLG
San Juan District Office (SJN-DO)
2/28/2002
29BGT99CARBONATED SOFT DRINK, N.E.C.
274COLOR LBLG
San Juan District Office (SJN-DO)
2/28/2002
30AFY99FRUIT BEVERAGE BASE, N.E.C.
274COLOR LBLG
San Juan District Office (SJN-DO)
2/28/2002
29BBY50SOFT DRINK, COLA, CARBONATED
218LIST INGRE
482NUTRIT LBL
San Juan District Office (SJN-DO)
2/28/2002
29BCY50SOFT DRINK, COLA, CARBONATED
218LIST INGRE
482NUTRIT LBL
San Juan District Office (SJN-DO)
10/3/2001
24KCT08PEPPER, HOT, WITH SAUCE
62NEEDS FCE
83NO PROCESS
Florida District Office (FLA-DO)

Frequently Asked Questions

What is C. I. Vega & Vega Ltda.'s FDA import refusal history?

C. I. Vega & Vega Ltda. (FEI: 3003400099) has 13 FDA import refusal record(s) in our database, spanning from 10/3/2001 to 10/30/2002.

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. C. I. Vega & Vega Ltda.'s FEI number is 3003400099.

What types of violations has C. I. Vega & Vega Ltda. received?

C. I. Vega & Vega Ltda. has been cited for 5 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 C. I. Vega & Vega Ltda. come from?

All FDA import refusal data for C. I. Vega & Vega Ltda. 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.