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Cooperativa Nacional De Productores De Leche

⚠️ Moderate Risk

FEI: 3001594351 • Montevideo, Montevideo • URUGUAY

FEI

FEI Number

3001594351

📍

Location

Montevideo, Montevideo

🇺🇾

Country

URUGUAY
🏢

Address

Magallanes 1871, , Montevideo, Montevideo, Uruguay

Moderate Risk

FDA Import Risk Assessment

35.3
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
2/3/2012
Latest Refusal
4/24/2007
Earliest Refusal

Score Breakdown

Violation Severity
66.7×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
8.4×10%
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

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.

2383×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

1561×

NO PERMIT

The article of milk or cream is not accompanied by a valid import milk permit, as required by the Federal Import Milk Act (21 U.S.C. 141-149).

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
2/3/2012
12AGP42CHEESE, PARMESAN
218LIST INGRE
238UNSAFE ADD
New York District Office (NYK-DO)
2/3/2012
12AGO52CHEESE, SEMISOFT
218LIST INGRE
238UNSAFE ADD
New York District Office (NYK-DO)
1/26/2012
12AGP42CHEESE, PARMESAN
218LIST INGRE
238UNSAFE ADD
New York District Office (NYK-DO)
4/24/2007
09CFT10MILK, VITAMIN D
156NO PERMIT
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Cooperativa Nacional De Productores De Leche's FDA import refusal history?

Cooperativa Nacional De Productores De Leche (FEI: 3001594351) has 4 FDA import refusal record(s) in our database, spanning from 4/24/2007 to 2/3/2012.

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. Cooperativa Nacional De Productores De Leche's FEI number is 3001594351.

What types of violations has Cooperativa Nacional De Productores De Leche received?

Cooperativa Nacional De Productores De Leche 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 Cooperativa Nacional De Productores De Leche come from?

All FDA import refusal data for Cooperativa Nacional De Productores De Leche 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.