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Coca Cola Beverage South Africa Proprietary Limited

⚠️ Moderate Risk

FEI: 3036656051 • Olifantsfontein, Gauteng • SOUTH AFRICA

FEI

FEI Number

3036656051

📍

Location

Olifantsfontein, Gauteng

🇿🇦
🏢

Address

15 Axle Dr., Clayville, Olifantsfontein, Gauteng, South Africa

Moderate Risk

FDA Import Risk Assessment

47.8
LowModerateHighCritical

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

Statistics

5
Total Refusals
3
Unique Violations
12/12/2025
Latest Refusal
12/11/2025
Earliest Refusal

Score Breakdown

Violation Severity
36.1×40%
Refusal Volume
28.8×30%
Recency
98.2×20%
Frequency
50.0×10%
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

3215×

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.

4825×

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.

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.

Refusal History

DateProductViolationsDivision
12/12/2025
29BET99CARBONATED SOFT DRINK, N.E.C.
321LACKS N/C
482NUTRIT LBL
Division of Southwest Imports (DSWI)
12/12/2025
29BET99CARBONATED SOFT DRINK, N.E.C.
218LIST INGRE
321LACKS N/C
482NUTRIT LBL
Division of Southwest Imports (DSWI)
12/11/2025
29BET99CARBONATED SOFT DRINK, N.E.C.
321LACKS N/C
482NUTRIT LBL
Division of Southwest Imports (DSWI)
12/11/2025
29BET99CARBONATED SOFT DRINK, N.E.C.
218LIST INGRE
321LACKS N/C
482NUTRIT LBL
Division of Southwest Imports (DSWI)
12/11/2025
29BET99CARBONATED SOFT DRINK, N.E.C.
218LIST INGRE
321LACKS N/C
482NUTRIT LBL
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is Coca Cola Beverage South Africa Proprietary Limited's FDA import refusal history?

Coca Cola Beverage South Africa Proprietary Limited (FEI: 3036656051) has 5 FDA import refusal record(s) in our database, spanning from 12/11/2025 to 12/12/2025.

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. Coca Cola Beverage South Africa Proprietary Limited's FEI number is 3036656051.

What types of violations has Coca Cola Beverage South Africa Proprietary Limited received?

Coca Cola Beverage South Africa Proprietary Limited has been cited for 3 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 Coca Cola Beverage South Africa Proprietary Limited come from?

All FDA import refusal data for Coca Cola Beverage South Africa Proprietary Limited 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.