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Montignac

⚠️ Moderate Risk

FEI: 3003748064 • London • UNITED KINGDOM

FEI

FEI Number

3003748064

📍

Location

London

🇬🇧
🏢

Address

160 Old Brompton Rd, , London, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

37.0
LowModerateHighCritical

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

Statistics

9
Total Refusals
4
Unique Violations
10/1/2002
Latest Refusal
10/1/2002
Earliest Refusal

Score Breakdown

Violation Severity
42.2×40%
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

3244×

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)).

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.

4822×

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.

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
10/1/2002
26AYY09VIRGIN OLIVE OIL, CRUDE
482NUTRIT LBL
New Orleans District Office (NOL-DO)
10/1/2002
22GYY99OTHER FRUIT AND FRUIT PRODUCTS, N.E.C.
482NUTRIT LBL
New Orleans District Office (NOL-DO)
10/1/2002
27VYY99VINEGAR, N.E.C.
324NO ENGLISH
New Orleans District Office (NOL-DO)
10/1/2002
04AYY05SPAGHETTI
324NO ENGLISH
New Orleans District Office (NOL-DO)
10/1/2002
34FYY02CHOCOLATE CANDY PIECES, WITHOUT NUTS AND FRUIT
324NO ENGLISH
New Orleans District Office (NOL-DO)
10/1/2002
22GYY99OTHER FRUIT AND FRUIT PRODUCTS, N.E.C.
324NO ENGLISH
New Orleans District Office (NOL-DO)
10/1/2002
03CYY99BREADS, ROLLS, BUNS, ETC N.E.C. PREPARED DRY MIX WITHOUT MILK OR EGG
249FILTHY
New Orleans District Office (NOL-DO)
10/1/2002
20KYY99CITRUS FRUIT, N.E.C., CITRUS FRUIT JUICES OR CONCENTRATES
218LIST INGRE
New Orleans District Office (NOL-DO)
10/1/2002
20KYY99CITRUS FRUIT, N.E.C., CITRUS FRUIT JUICES OR CONCENTRATES
218LIST INGRE
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Montignac's FDA import refusal history?

Montignac (FEI: 3003748064) has 9 FDA import refusal record(s) in our database, spanning from 10/1/2002 to 10/1/2002.

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. Montignac's FEI number is 3003748064.

What types of violations has Montignac received?

Montignac has been cited for 4 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 Montignac come from?

All FDA import refusal data for Montignac 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.