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SHENZHEN BANGXING RUBBER TECHNOLOGY .CO.LTD.

✅ Low Risk

FEI: 3015187858 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3015187858

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Building Xiakeng Second F/4, B2 Tongle Community, Longgang; Industrial Area, Shenzhen, Guangdong, China

Low Risk

FDA Import Risk Assessment

24.4
LowModerateHighCritical

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

Statistics

2
Total Refusals
6
Unique Violations
5/16/2018
Latest Refusal
3/4/2015
Earliest Refusal

Score Breakdown

Violation Severity
46.3×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
6.2×10%
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

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32802×

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.

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

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.

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

4841×

DV NAME

The article appears to be a device and its labeling fails to bear the proprietary or established name.

Refusal History

DateProductViolationsDivision
5/16/2018
76MEFRING, TEETHING, NON-FLUID FILLED
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
3/4/2015
76MEFRING, TEETHING, NON-FLUID FILLED
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
341REGISTERED
484DV NAME
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SHENZHEN BANGXING RUBBER TECHNOLOGY .CO.LTD.'s FDA import refusal history?

SHENZHEN BANGXING RUBBER TECHNOLOGY .CO.LTD. (FEI: 3015187858) has 2 FDA import refusal record(s) in our database, spanning from 3/4/2015 to 5/16/2018.

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. SHENZHEN BANGXING RUBBER TECHNOLOGY .CO.LTD.'s FEI number is 3015187858.

What types of violations has SHENZHEN BANGXING RUBBER TECHNOLOGY .CO.LTD. received?

SHENZHEN BANGXING RUBBER TECHNOLOGY .CO.LTD. has been cited for 6 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 SHENZHEN BANGXING RUBBER TECHNOLOGY .CO.LTD. come from?

All FDA import refusal data for SHENZHEN BANGXING RUBBER TECHNOLOGY .CO.LTD. 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.