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Radiant Technologies

⚠️ Moderate Risk

FEI: 3004148384 • Johannesburg, Gauteng • SOUTH AFRICA

FEI

FEI Number

3004148384

📍

Location

Johannesburg, Gauteng

🇿🇦
🏢

Address

12 Atholl Road, , Johannesburg, Gauteng, South Africa

Moderate Risk

FDA Import Risk Assessment

38.7
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
10/18/2005
Latest Refusal
5/25/2004
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
14.3×10%
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

21201×

UNSFDIETSP

The article appears to be a dietary supplement or ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury.

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

Refusal History

DateProductViolationsDivision
10/18/2005
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
2120UNSFDIETSP
Los Angeles District Office (LOS-DO)
5/25/2004
54BCL99MINERAL N.E.C.
62NEEDS FCE
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Radiant Technologies's FDA import refusal history?

Radiant Technologies (FEI: 3004148384) has 2 FDA import refusal record(s) in our database, spanning from 5/25/2004 to 10/18/2005.

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. Radiant Technologies's FEI number is 3004148384.

What types of violations has Radiant Technologies received?

Radiant Technologies 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 Radiant Technologies come from?

All FDA import refusal data for Radiant Technologies 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.