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OMAN REFRESHMENT COMPANY

⚠️ Moderate Risk

FEI: 3025831286 • Cpo Airport • OMAN

FEI

FEI Number

3025831286

📍

Location

Cpo Airport

🇴🇲

Country

OMAN
🏢

Address

111 Postal Code, Po Box 30, Cpo Airport, , Oman

Moderate Risk

FDA Import Risk Assessment

35.8
LowModerateHighCritical

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

Statistics

2
Total Refusals
5
Unique Violations
7/26/2023
Latest Refusal
7/26/2023
Earliest Refusal

Score Breakdown

Violation Severity
46.0×40%
Refusal Volume
17.7×30%
Recency
50.7×20%
Frequency
20.0×10%
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

112×

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).

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.

3202×

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.

3212×

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.

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.

Refusal History

DateProductViolationsDivision
7/26/2023
29BET60SODA WATER, CARBONATED
11UNSAFE COL
218LIST INGRE
320LACKS FIRM
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
7/26/2023
29BET60SODA WATER, CARBONATED
11UNSAFE COL
218LIST INGRE
320LACKS FIRM
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

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

OMAN REFRESHMENT COMPANY (FEI: 3025831286) has 2 FDA import refusal record(s) in our database, spanning from 7/26/2023 to 7/26/2023.

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 3025831286.

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.