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IMOIL

⚠️ Moderate Risk

FEI: 3004230628 • Itri • ITALY

FEI

FEI Number

3004230628

📍

Location

Itri

🇮🇹

Country

ITALY
🏢

Address

St.prov. Itri-sperlonga Km 1400, , Itri, , Italy

Moderate Risk

FDA Import Risk Assessment

33.6
LowModerateHighCritical

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

Statistics

8
Total Refusals
6
Unique Violations
1/20/2004
Latest Refusal
1/20/2004
Earliest Refusal

Score Breakdown

Violation Severity
37.5×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
80.0×10%
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)).

2564×

INCONSPICU

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)).

4734×

LABELING

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

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.

2181×

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.

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
1/20/2004
26ACT04OLIVE OIL, CRUDE (FOR REFINING)
324NO ENGLISH
473LABELING
482NUTRIT LBL
Detroit District Office (DET-DO)
1/20/2004
26CCT04OLIVE OIL, REFINED, SINGLE INGREDIENT
324NO ENGLISH
473LABELING
482NUTRIT LBL
Detroit District Office (DET-DO)
1/20/2004
26CCT04OLIVE OIL, REFINED, SINGLE INGREDIENT
324NO ENGLISH
473LABELING
482NUTRIT LBL
Detroit District Office (DET-DO)
1/20/2004
23MHT99EDIBLE SEED PRODUCTS, N.E.C.
324NO ENGLISH
473LABELING
Detroit District Office (DET-DO)
1/20/2004
23MHT99EDIBLE SEED PRODUCTS, N.E.C.
256INCONSPICU
324NO ENGLISH
Detroit District Office (DET-DO)
1/20/2004
21GHT09OLIVES (PIT FRUIT)
256INCONSPICU
324NO ENGLISH
Detroit District Office (DET-DO)
1/20/2004
21GHT09OLIVES (PIT FRUIT)
249FILTHY
256INCONSPICU
324NO ENGLISH
Detroit District Office (DET-DO)
1/20/2004
26AET04OLIVE OIL, CRUDE (FOR REFINING)
218LIST INGRE
256INCONSPICU
Detroit District Office (DET-DO)

Frequently Asked Questions

What is IMOIL's FDA import refusal history?

IMOIL (FEI: 3004230628) has 8 FDA import refusal record(s) in our database, spanning from 1/20/2004 to 1/20/2004.

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. IMOIL's FEI number is 3004230628.

What types of violations has IMOIL received?

IMOIL has been cited for 6 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 IMOIL come from?

All FDA import refusal data for IMOIL 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.