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NINGBO ZHONGXIN ELECTRONICS

⚠️ Moderate Risk

FEI: 3012680905 • Ningbo, Zhejiang • CHINA

FEI

FEI Number

3012680905

📍

Location

Ningbo, Zhejiang

🇨🇳

Country

CHINA
🏢

Address

No 132 Ren Min Road, , Ningbo, Zhejiang, China

Moderate Risk

FDA Import Risk Assessment

27.5
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
10/7/2016
Latest Refusal
10/7/2016
Earliest Refusal

Score Breakdown

Violation Severity
58.0×40%
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

1181×

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).

2881×

STD LABEL

The article appears to not bear labeling prescribed by the performance standard established under section 514.

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.

471×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
10/7/2016
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
288STD LABEL
3280FRNMFGREG
47NON STD
508NO 510(K)
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is NINGBO ZHONGXIN ELECTRONICS's FDA import refusal history?

NINGBO ZHONGXIN ELECTRONICS (FEI: 3012680905) has 1 FDA import refusal record(s) in our database, spanning from 10/7/2016 to 10/7/2016.

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. NINGBO ZHONGXIN ELECTRONICS's FEI number is 3012680905.

What types of violations has NINGBO ZHONGXIN ELECTRONICS received?

NINGBO ZHONGXIN ELECTRONICS has been cited for 5 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 NINGBO ZHONGXIN ELECTRONICS come from?

All FDA import refusal data for NINGBO ZHONGXIN ELECTRONICS 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.