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HUIZHOU XIAOOU TECHNOLOGY CO.,LTD.

⚠️ Moderate Risk

FEI: 3016664338 • Huizhou, Guangdong • CHINA

FEI

FEI Number

3016664338

📍

Location

Huizhou, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Xikengindustrial 3rd Floor, No. 113 Zhongkai High-Tech; Zone Zone (Plant D), Huizhou, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

35.0
LowModerateHighCritical

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

Statistics

5
Total Refusals
5
Unique Violations
4/21/2021
Latest Refusal
7/7/2020
Earliest Refusal

Score Breakdown

Violation Severity
53.3×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
50.0×10%
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

1183×

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.

5082×

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.

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.

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).

Refusal History

DateProductViolationsDivision
4/21/2021
80PXHTHERMOMETER KIT
341REGISTERED
Division of West Coast Imports (DWCI)
2/2/2021
80PXHTHERMOMETER KIT
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
12/15/2020
80FLLTHERMOMETER, ELECTRONIC, CLINICAL
118NOT LISTED
3280FRNMFGREG
Division of West Coast Imports (DWCI)
8/19/2020
80PXHTHERMOMETER KIT
118NOT LISTED
223FALSE
508NO 510(K)
Division of Southwest Imports (DSWI)
7/7/2020
80PXHTHERMOMETER KIT
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is HUIZHOU XIAOOU TECHNOLOGY CO.,LTD.'s FDA import refusal history?

HUIZHOU XIAOOU TECHNOLOGY CO.,LTD. (FEI: 3016664338) has 5 FDA import refusal record(s) in our database, spanning from 7/7/2020 to 4/21/2021.

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. HUIZHOU XIAOOU TECHNOLOGY CO.,LTD.'s FEI number is 3016664338.

What types of violations has HUIZHOU XIAOOU TECHNOLOGY CO.,LTD. received?

HUIZHOU XIAOOU TECHNOLOGY CO.,LTD. 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 HUIZHOU XIAOOU TECHNOLOGY CO.,LTD. come from?

All FDA import refusal data for HUIZHOU XIAOOU 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.