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Om Export Company

⚠️ Moderate Risk

FEI: 3011562286 • Ahmedabad, Gujarat • INDIA

FEI

FEI Number

3011562286

📍

Location

Ahmedabad, Gujarat

🇮🇳

Country

INDIA
🏢

Address

E - 43 Hariom Flat, Jaiambenagar, Ahmedabad, Gujarat, India

Moderate Risk

FDA Import Risk Assessment

39.7
LowModerateHighCritical

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

Statistics

8
Total Refusals
10
Unique Violations
3/18/2024
Latest Refusal
12/15/2015
Earliest Refusal

Score Breakdown

Violation Severity
45.7×40%
Refusal Volume
35.3×30%
Recency
49.4×20%
Frequency
9.7×10%
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

4733×

LABELING

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

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.

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

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.

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)).

38811×

COSMETFPLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain an undeclared color additive which renders it misbranded within the meaning of Sections 1454(c)(3)(B) and 1456 of the Fair Packaging and Labeling Act.

4711×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

4821×

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.

1971×

COSM COLOR

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).

Refusal History

DateProductViolationsDivision
3/18/2024
53IY02MOUTHWASHES AND BREATH FRESHENERS (LIQUIDS AND SPRAYS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS)
197COSM COLOR
3881COSMETFPLA
471CSTIC LBLG
473LABELING
Division of Northeast Imports (DNEI)
7/13/2023
36AYT99SUGAR PRODUCTS, N.E.C.
11UNSAFE COL
274COLOR LBLG
Division of Northeast Imports (DNEI)
9/28/2017
07BGT99FRIED SNACK FOODS, N.E.C.
473LABELING
Division of Northeast Imports (DNEI)
9/6/2017
07BGT06POTATO CHIPS,FRIED
473LABELING
Division of Northeast Imports (DNEI)
9/6/2017
28BGT08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), GROUND, CRACKED (SPICE)
218LIST INGRE
Division of Northeast Imports (DNEI)
9/6/2017
30YGT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C.
218LIST INGRE
Division of Northeast Imports (DNEI)
6/16/2016
28EGT99MIXED SPICE AND SEAONINGS, WITHOUT SALT, N.E.C.
324NO ENGLISH
New York District Office (NYK-DO)
12/15/2015
33EGT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
218LIST INGRE
320LACKS FIRM
482NUTRIT LBL
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Om Export Company's FDA import refusal history?

Om Export Company (FEI: 3011562286) has 8 FDA import refusal record(s) in our database, spanning from 12/15/2015 to 3/18/2024.

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. Om Export Company's FEI number is 3011562286.

What types of violations has Om Export Company received?

Om Export Company 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 Om Export Company come from?

All FDA import refusal data for Om Export Company 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.