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Smithkline Beecham Consumer

⚠️ Moderate Risk

FEI: 1000163864 • Slough • UNITED KINGDOM

FEI

FEI Number

1000163864

📍

Location

Slough

🇬🇧
🏢

Address

11 Stoke Poges Lane, , Slough, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

25.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
12/1/2003
Latest Refusal
12/1/2003
Earliest Refusal

Score Breakdown

Violation Severity
52.5×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

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).

2741×

COLOR LBLG

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

4731×

LABELING

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

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.

Refusal History

DateProductViolationsDivision
12/1/2003
29BEY02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED
11UNSAFE COL
274COLOR LBLG
473LABELING
482NUTRIT LBL
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Smithkline Beecham Consumer's FDA import refusal history?

Smithkline Beecham Consumer (FEI: 1000163864) has 1 FDA import refusal record(s) in our database, spanning from 12/1/2003 to 12/1/2003.

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. Smithkline Beecham Consumer's FEI number is 1000163864.

What types of violations has Smithkline Beecham Consumer received?

Smithkline Beecham Consumer has been cited for 4 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 Smithkline Beecham Consumer come from?

All FDA import refusal data for Smithkline Beecham Consumer 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.