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Brightime Intertrade Ltd Part

✅ Low Risk

FEI: 3002350561 • Bangkok • THAILAND

FEI

FEI Number

3002350561

📍

Location

Bangkok

🇹🇭

Country

THAILAND
🏢

Address

78 Phatthanakarn 54, , Bangkok, , Thailand

Low Risk

FDA Import Risk Assessment

19.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
2/21/2013
Latest Refusal
2/21/2013
Earliest Refusal

Score Breakdown

Violation Severity
30.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

3202×

LACKS FIRM

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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
2/21/2013
28BGT99SPICES, GROUND, CRACKED, ETC., N.E.C.
320LACKS FIRM
Division of Northeast Imports (DNEI)
2/21/2013
28BGT99SPICES, GROUND, CRACKED, ETC., N.E.C.
320LACKS FIRM
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Brightime Intertrade Ltd Part's FDA import refusal history?

Brightime Intertrade Ltd Part (FEI: 3002350561) has 2 FDA import refusal record(s) in our database, spanning from 2/21/2013 to 2/21/2013.

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. Brightime Intertrade Ltd Part's FEI number is 3002350561.

What types of violations has Brightime Intertrade Ltd Part received?

Brightime Intertrade Ltd Part has been cited for 1 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 Brightime Intertrade Ltd Part come from?

All FDA import refusal data for Brightime Intertrade Ltd Part 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.