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Nestle De Mexico Sa De Cv

⚠️ Moderate Risk

FEI: 3003215801 • D.F. • MEXICO

FEI

FEI Number

3003215801

📍

Location

D.F.

🇲🇽

Country

MEXICO
🏢

Address

Ave. Ejercito Nacional 435, , Mexico, D.F., , Mexico

Moderate Risk

FDA Import Risk Assessment

35.8
LowModerateHighCritical

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

Statistics

9
Total Refusals
7
Unique Violations
12/5/2005
Latest Refusal
2/24/2003
Earliest Refusal

Score Breakdown

Violation Severity
53.6×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
32.4×10%
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

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.

832×

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.

622×

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).

2542×

STD QUALIT

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(h)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a standard of quality has been prescribed by regulation as provided by Section 401 of the FD&C Act, and its quality falls below such standard and its label does not bear a statement that it falls below such standard in such manner and form as such regulations specify.

3241×

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)).

4881×

HEALTH C

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 bears an unauthorized nutrient content/health claim.

Refusal History

DateProductViolationsDivision
12/5/2005
09CHT11MILK WITH MULTIVITAMINS ADDED
488HEALTH C
Southwest Import District Office (SWI-DO)
4/14/2004
40CDE01MILK BASE FORMULA PRODUCT (BABY)
254STD QUALIT
Southwest Import District Office (SWI-DO)
3/24/2004
40CDE01MILK BASE FORMULA PRODUCT (BABY)
254STD QUALIT
Southwest Import District Office (SWI-DO)
2/23/2004
09EDE16DRIED MILK, NON FAT
218LIST INGRE
482NUTRIT LBL
Southwest Import District Office (SWI-DO)
2/23/2004
09EDE16DRIED MILK, NON FAT
218LIST INGRE
482NUTRIT LBL
Southwest Import District Office (SWI-DO)
2/17/2004
09EDE16DRIED MILK, NON FAT
218LIST INGRE
482NUTRIT LBL
Southwest Import District Office (SWI-DO)
3/7/2003
14BYY04IMITATION MILK, CHEESE TYPE PRODUCT (SOY CHEESE, ETC.)
62NEEDS FCE
83NO PROCESS
Southwest Import District Office (SWI-DO)
3/7/2003
14BYY04IMITATION MILK, CHEESE TYPE PRODUCT (SOY CHEESE, ETC.)
62NEEDS FCE
83NO PROCESS
Southwest Import District Office (SWI-DO)
2/24/2003
40CET01MILK BASE FORMULA PRODUCT (BABY)
324NO ENGLISH
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Nestle De Mexico Sa De Cv's FDA import refusal history?

Nestle De Mexico Sa De Cv (FEI: 3003215801) has 9 FDA import refusal record(s) in our database, spanning from 2/24/2003 to 12/5/2005.

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 Mexico Sa De Cv's FEI number is 3003215801.

What types of violations has Nestle De Mexico Sa De Cv received?

Nestle De Mexico Sa De Cv 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 Nestle De Mexico Sa De Cv come from?

All FDA import refusal data for Nestle De Mexico Sa De Cv 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.