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OMAN REFRESHMENT COMPANY

⚠️ Moderate Risk

FEI: 3025812467 • Bowsher, OM-MA • OMAN

FEI

FEI Number

3025812467

📍

Location

Bowsher, OM-MA

🇴🇲

Country

OMAN
🏢

Address

234 Al Ghubrah Street, , Bowsher, OM-MA, Oman

Moderate Risk

FDA Import Risk Assessment

45.5
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
9/4/2024
Latest Refusal
9/4/2024
Earliest Refusal

Score Breakdown

Violation Severity
47.8×40%
Refusal Volume
25.9×30%
Recency
72.9×20%
Frequency
40.0×10%
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

114×

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).

2744×

COLOR LBLG

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

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.

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.

3242×

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)).

Refusal History

DateProductViolationsDivision
9/4/2024
29BCT50SOFT DRINK, COLA, CARBONATED
11UNSAFE COL
274COLOR LBLG
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
9/4/2024
29BCT50SOFT DRINK, COLA, CARBONATED
11UNSAFE COL
274COLOR LBLG
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
9/4/2024
29BCT50SOFT DRINK, COLA, CARBONATED
11UNSAFE COL
274COLOR LBLG
321LACKS N/C
324NO ENGLISH
482NUTRIT LBL
Division of Northeast Imports (DNEI)
9/4/2024
29BCT50SOFT DRINK, COLA, CARBONATED
11UNSAFE COL
274COLOR LBLG
321LACKS N/C
324NO ENGLISH
482NUTRIT LBL
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is OMAN REFRESHMENT COMPANY's FDA import refusal history?

OMAN REFRESHMENT COMPANY (FEI: 3025812467) has 4 FDA import refusal record(s) in our database, spanning from 9/4/2024 to 9/4/2024.

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. OMAN REFRESHMENT COMPANY's FEI number is 3025812467.

What types of violations has OMAN REFRESHMENT COMPANY received?

OMAN REFRESHMENT COMPANY has been cited for 5 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 OMAN REFRESHMENT COMPANY come from?

All FDA import refusal data for OMAN REFRESHMENT 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.