ImportRefusal LogoImportRefusal

Mondizen

⚠️ Moderate Risk

FEI: 3008723861 • LA Cote St Andre, Isere • FRANCE

FEI

FEI Number

3008723861

📍

Location

LA Cote St Andre, Isere

🇫🇷

Country

FRANCE
🏢

Address

300 Rue Georges Brassens, , LA Cote St Andre, Isere, France

Moderate Risk

FDA Import Risk Assessment

37.5
LowModerateHighCritical

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

Statistics

9
Total Refusals
10
Unique Violations
1/17/2012
Latest Refusal
9/16/2011
Earliest Refusal

Score Breakdown

Violation Severity
43.3×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
90.0×10%
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

3247×

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)).

4824×

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.

2184×

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.

3214×

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.

3284×

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.

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).

33611×

NUTR DEF

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the infant formula appears to adulterated in that it does not provide the nutrients required by 21 CFR 107.100

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.

4731×

LABELING

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

Refusal History

DateProductViolationsDivision
1/17/2012
40YGT99BABY AND JUNIOR FOOD N.E.C.
218LIST INGRE
321LACKS N/C
324NO ENGLISH
328USUAL NAME
482NUTRIT LBL
New York District Office (NYK-DO)
1/17/2012
40BGT99CEREAL, N.E.C. (BABY)
218LIST INGRE
321LACKS N/C
324NO ENGLISH
328USUAL NAME
482NUTRIT LBL
New York District Office (NYK-DO)
1/17/2012
40NET99OTHER FORMULA PRODUCTS, N.E.C., READY TO FEED
218LIST INGRE
321LACKS N/C
324NO ENGLISH
328USUAL NAME
482NUTRIT LBL
New York District Office (NYK-DO)
1/17/2012
40DEE99VEGETABLES, N.E.C. (BABY)
218LIST INGRE
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
328USUAL NAME
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
12/20/2011
40EET20MIXED FRUIT (BABY)
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
12/16/2011
03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C.
473LABELING
New York District Office (NYK-DO)
12/16/2011
40DGT99VEGETABLES, N.E.C. (BABY)
324NO ENGLISH
New York District Office (NYK-DO)
12/16/2011
40YGT99BABY AND JUNIOR FOOD N.E.C.
324NO ENGLISH
New York District Office (NYK-DO)
9/16/2011
40CET01MILK BASE FORMULA PRODUCT (BABY)
324NO ENGLISH
3361NUTR DEF
New York District Office (NYK-DO)

Frequently Asked Questions

What is Mondizen's FDA import refusal history?

Mondizen (FEI: 3008723861) has 9 FDA import refusal record(s) in our database, spanning from 9/16/2011 to 1/17/2012.

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. Mondizen's FEI number is 3008723861.

What types of violations has Mondizen received?

Mondizen has been cited for 10 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 Mondizen come from?

All FDA import refusal data for Mondizen 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.