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SHENZHEN ZHIDA XINTAI TECHNOLOGYCO

⚠️ Moderate Risk

FEI: 3031410026 • Shenzhen • CHINA

FEI

FEI Number

3031410026

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

No 1 Longjin 2 Rd, Xinan Street, Unit 501-501q, Dong Jiang Hao Yuan, Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

43.6
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
2/7/2025
Latest Refusal
2/7/2025
Earliest Refusal

Score Breakdown

Violation Severity
57.5×40%
Refusal Volume
11.2×30%
Recency
81.2×20%
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).

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

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.

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
2/7/2025
80FLESTERILIZER, STEAM
118NOT LISTED
223FALSE
3280FRNMFGREG
508NO 510(K)
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is SHENZHEN ZHIDA XINTAI TECHNOLOGYCO's FDA import refusal history?

SHENZHEN ZHIDA XINTAI TECHNOLOGYCO (FEI: 3031410026) has 1 FDA import refusal record(s) in our database, spanning from 2/7/2025 to 2/7/2025.

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 ZHIDA XINTAI TECHNOLOGYCO's FEI number is 3031410026.

What types of violations has SHENZHEN ZHIDA XINTAI TECHNOLOGYCO received?

SHENZHEN ZHIDA XINTAI TECHNOLOGYCO has been cited for 4 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 ZHIDA XINTAI TECHNOLOGYCO come from?

All FDA import refusal data for SHENZHEN ZHIDA XINTAI TECHNOLOGYCO 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.