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Heidi London

⚠️ Moderate Risk

FEI: 3009602557 • London • UNITED KINGDOM

FEI

FEI Number

3009602557

📍

Location

London

🇬🇧
🏢

Address

Studio 5 53-84 Aldgate High St, , London, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

26.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
1/14/2015
Latest Refusal
1/14/2015
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
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

2351×

NOT IMPACT

The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
1/14/2015
86HQZFRAME, SPECTACLE
235NOT IMPACT
3280FRNMFGREG
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Heidi London's FDA import refusal history?

Heidi London (FEI: 3009602557) has 1 FDA import refusal record(s) in our database, spanning from 1/14/2015 to 1/14/2015.

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. Heidi London's FEI number is 3009602557.

What types of violations has Heidi London received?

Heidi London 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 Heidi London come from?

All FDA import refusal data for Heidi London 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.