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Euroasias

⚠️ High Risk

FEI: 3010070733 • Mumbai, Maharashtra • INDIA

FEI

FEI Number

3010070733

📍

Location

Mumbai, Maharashtra

🇮🇳

Country

INDIA
🏢

Address

207 Parvati Industrial Estate, , Mumbai, Maharashtra, India

High Risk

FDA Import Risk Assessment

64.6
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

12
Total Refusals
7
Unique Violations
3/26/2024
Latest Refusal
2/20/2020
Earliest Refusal

Score Breakdown

Violation Severity
91.2×40%
Refusal Volume
41.3×30%
Recency
64.1×20%
Frequency
29.3×10%
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

2498×

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.

97×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

1576×

FOREIGN OB

The article appears to consist in whole or in part of a filthy, putrid, or decomposed substance, or is otherwise unfit for food in that it appears to contain foreign objects.

38971×

MYCOTOXIN

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous and deleterious substance, namely a mycotoxin (aflatoxin, deoxynivalenol, fumonisin, or ochratoxin A), which may render it injurious to health. Bears or contains:

2561×

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)).

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.

34001×

PB-FOOD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a poisonous or deleterious substance, lead, which may render it injurious to health.

Refusal History

DateProductViolationsDivision
3/26/2024
28GYH04CURRY POWDER, LIQUID, WITHOUT SALT
3400PB-FOOD
Division of Northeast Imports (DNEI)
5/12/2022
28BET30NUTMEG, GROUND, CRACKED (SPICE)
3897MYCOTOXIN
Division of Northeast Imports (DNEI)
7/30/2021
28BYH54PEPPER, BLACK, GROUND, CRACKED (SPICE)
249FILTHY
Division of Northeast Imports (DNEI)
7/1/2021
28BYH54PEPPER, BLACK, GROUND, CRACKED (SPICE)
157FOREIGN OB
249FILTHY
9SALMONELLA
Division of Northeast Imports (DNEI)
7/1/2021
28BYH54PEPPER, BLACK, GROUND, CRACKED (SPICE)
157FOREIGN OB
249FILTHY
9SALMONELLA
Division of Northeast Imports (DNEI)
5/10/2021
28BYH54PEPPER, BLACK, GROUND, CRACKED (SPICE)
157FOREIGN OB
249FILTHY
9SALMONELLA
Division of Northeast Imports (DNEI)
5/10/2021
28BYY54PEPPER, BLACK, GROUND, CRACKED (SPICE)
157FOREIGN OB
249FILTHY
9SALMONELLA
Division of Northeast Imports (DNEI)
5/10/2021
28BYH54PEPPER, BLACK, GROUND, CRACKED (SPICE)
157FOREIGN OB
249FILTHY
9SALMONELLA
Division of Northeast Imports (DNEI)
5/7/2021
28BYH54PEPPER, BLACK, GROUND, CRACKED (SPICE)
157FOREIGN OB
249FILTHY
9SALMONELLA
Division of Northeast Imports (DNEI)
9/4/2020
21TYH14TAMARIND, DRIED OR PASTE
249FILTHY
Division of Northeast Imports (DNEI)
5/14/2020
22BYY05BITTER MELON, DRIED OR PASTE
218LIST INGRE
256INCONSPICU
Division of Northeast Imports (DNEI)
2/20/2020
28AYH54PEPPER,BLACK, WHOLE (SPICE)
9SALMONELLA
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Euroasias's FDA import refusal history?

Euroasias (FEI: 3010070733) has 12 FDA import refusal record(s) in our database, spanning from 2/20/2020 to 3/26/2024.

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. Euroasias's FEI number is 3010070733.

What types of violations has Euroasias received?

Euroasias 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 Euroasias come from?

All FDA import refusal data for Euroasias 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.