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BFL METAL PRODUCTION

⚠️ Moderate Risk

FEI: 3015999462 • Central • HONG KONG

FEI

FEI Number

3015999462

📍

Location

Central

🇭🇰

Country

HONG KONG
🏢

Address

1903 Hing Yip Des Voeux, , Central, , Hong Kong

Moderate Risk

FDA Import Risk Assessment

37.9
LowModerateHighCritical

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

Statistics

6
Total Refusals
3
Unique Violations
12/14/2021
Latest Refusal
11/12/2021
Earliest Refusal

Score Breakdown

Violation Severity
54.3×40%
Refusal Volume
31.3×30%
Recency
4.0×20%
Frequency
60.0×10%
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

38426×

TP NO PMTA

This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act because it is a tobacco product that FDA has found to be adulterated under section 902(6)(A) of the FD&C Act in that it does not have an FDA marketing order in effect under section 910(c)(1)(A)(i) of the FD&C Act.

38436×

TP NO SE

This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act because it is a tobacco product that FDA has found to be misbranded under section 903(a)(6) of the FD&C Act in that a notice or other information respecting it was not provided as required by section 905(j).

38542×

TPLKUSSLLB

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(D) of the FD&C Act in that the label does not provide the statement "sale only allowed in the United States" and the tobacco product is not subject to any exemptions or variations.

Refusal History

DateProductViolationsDivision
12/14/2021
98MAA99ELECTRONIC NICOTINE DELIVERY SYSTEM COMPONENT/PART, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
11/16/2021
98MAA99ELECTRONIC NICOTINE DELIVERY SYSTEM COMPONENT/PART, NEC
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
11/16/2021
98MAA99ELECTRONIC NICOTINE DELIVERY SYSTEM COMPONENT/PART, NEC
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
11/12/2021
98MAA99ELECTRONIC NICOTINE DELIVERY SYSTEM COMPONENT/PART, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
11/12/2021
98MAA99ELECTRONIC NICOTINE DELIVERY SYSTEM COMPONENT/PART, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
11/12/2021
98MAA99ELECTRONIC NICOTINE DELIVERY SYSTEM COMPONENT/PART, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is BFL METAL PRODUCTION's FDA import refusal history?

BFL METAL PRODUCTION (FEI: 3015999462) has 6 FDA import refusal record(s) in our database, spanning from 11/12/2021 to 12/14/2021.

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. BFL METAL PRODUCTION's FEI number is 3015999462.

What types of violations has BFL METAL PRODUCTION received?

BFL METAL PRODUCTION has been cited for 3 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 BFL METAL PRODUCTION come from?

All FDA import refusal data for BFL METAL PRODUCTION 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.