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Sun Essences

✅ Low Risk

FEI: 3004024625 • Colby Norwich • UNITED KINGDOM

FEI

FEI Number

3004024625

📍

Location

Colby Norwich

🇬🇧
🏢

Address

7 Church Rd Well C, , Colby Norwich, , United Kingdom

Low Risk

FDA Import Risk Assessment

22.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
2
Unique Violations
2/25/2004
Latest Refusal
2/25/2004
Earliest Refusal

Score Breakdown

Violation Severity
45.0×40%
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

3311×

DR QUALITC

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the drug appears to be represented as not being recognized in an official compendium and appears its strength differs from or its quality or purity falls below, that which it purports or is represented to possess.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
2/25/2004
66VAS99MISCELLANEOUS PATENT MEDICINES, ETC.
331DR QUALITC
333LACKS FIRM
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Sun Essences's FDA import refusal history?

Sun Essences (FEI: 3004024625) has 1 FDA import refusal record(s) in our database, spanning from 2/25/2004 to 2/25/2004.

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. Sun Essences's FEI number is 3004024625.

What types of violations has Sun Essences received?

Sun Essences has been cited for 2 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 Sun Essences come from?

All FDA import refusal data for Sun Essences 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.