ImportRefusal LogoImportRefusal

HARBIN XIANDE TECHNOLOGY DEVELOPMENT CO., LTD.

⚠️ Moderate Risk

FEI: 3016823635 • Harbin City, Heilongjiang • CHINA

FEI

FEI Number

3016823635

📍

Location

Harbin City, Heilongjiang

🇨🇳

Country

CHINA
🏢

Address

No. 434 Youzheng Street, Nangang District, Harbin City, Heilongjiang, China

Moderate Risk

FDA Import Risk Assessment

36.7
LowModerateHighCritical

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

Statistics

5
Total Refusals
3
Unique Violations
9/30/2020
Latest Refusal
7/6/2020
Earliest Refusal

Score Breakdown

Violation Severity
57.7×40%
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

5085×

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.

1184×

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).

32804×

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.

Refusal History

DateProductViolationsDivision
9/30/2020
80FQZTHERMOMETER, CLINICAL COLOR CHANGE
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
9/30/2020
80FQZTHERMOMETER, CLINICAL COLOR CHANGE
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
9/9/2020
80FLLTHERMOMETER, ELECTRONIC, CLINICAL
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
8/31/2020
80FLLTHERMOMETER, ELECTRONIC, CLINICAL
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
7/6/2020
80FLKTHERMOMETER, CLINICAL MERCURY
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is HARBIN XIANDE TECHNOLOGY DEVELOPMENT CO., LTD.'s FDA import refusal history?

HARBIN XIANDE TECHNOLOGY DEVELOPMENT CO., LTD. (FEI: 3016823635) has 5 FDA import refusal record(s) in our database, spanning from 7/6/2020 to 9/30/2020.

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. HARBIN XIANDE TECHNOLOGY DEVELOPMENT CO., LTD.'s FEI number is 3016823635.

What types of violations has HARBIN XIANDE TECHNOLOGY DEVELOPMENT CO., LTD. received?

HARBIN XIANDE TECHNOLOGY DEVELOPMENT CO., LTD. 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 HARBIN XIANDE TECHNOLOGY DEVELOPMENT CO., LTD. come from?

All FDA import refusal data for HARBIN XIANDE TECHNOLOGY DEVELOPMENT 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.