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Huajia (Tianjin) International

⚠️ Moderate Risk

FEI: 3004645875 • Beijing • CHINA

FEI

FEI Number

3004645875

📍

Location

Beijing

🇨🇳

Country

CHINA
🏢

Address

No.8 South Street Of Waijiaobu, , Beijing, , China

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
1/11/2008
Latest Refusal
1/11/2008
Earliest Refusal

Score Breakdown

Violation Severity
52.5×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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).

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).

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.

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
1/11/2008
76EFWTOOTHBRUSH, MANUAL
118NOT LISTED
341REGISTERED
Minneapolis District Office (MIN-DO)
1/11/2008
95L22LASER PRODUCT FOR NON-MEDICAL USE
47NON STD
476NO REGISTR
Minneapolis District Office (MIN-DO)

Frequently Asked Questions

What is Huajia (Tianjin) International's FDA import refusal history?

Huajia (Tianjin) International (FEI: 3004645875) has 2 FDA import refusal record(s) in our database, spanning from 1/11/2008 to 1/11/2008.

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. Huajia (Tianjin) International's FEI number is 3004645875.

What types of violations has Huajia (Tianjin) International received?

Huajia (Tianjin) International 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 Huajia (Tianjin) International come from?

All FDA import refusal data for Huajia (Tianjin) International 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.