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SHENZHEN FIRST UNION TECHNOLOGY CO., LTD.

⚠️ Moderate Risk

FEI: 3007522015 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3007522015

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

4-5 F, Bldg. A, Xingbao Industry Zone, No. 60 Xin'an Rd., Block 22, Bao'an Dist, Shenzhen, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

38.0
LowModerateHighCritical

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

Statistics

5
Total Refusals
4
Unique Violations
5/4/2010
Latest Refusal
12/8/2008
Earliest Refusal

Score Breakdown

Violation Severity
64.4×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
35.6×10%
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

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).

753×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

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
5/4/2010
80LDQDEVICE, GENERAL MEDICAL
118NOT LISTED
341REGISTERED
75UNAPPROVED
Los Angeles District Office (LOS-DO)
8/17/2009
66BAS44NICOTINE DELIVERY SYSTEM
75UNAPPROVED
Cincinnati District Office (CIN-DO)
4/20/2009
66BBY44NICOTINE DELIVERY SYSTEM
118NOT LISTED
237NO PMA
75UNAPPROVED
Seattle District Office (SEA-DO)
12/8/2008
66BAS44NICOTINE DELIVERY SYSTEM
118NOT LISTED
Cincinnati District Office (CIN-DO)
12/8/2008
66BAS44NICOTINE DELIVERY SYSTEM
118NOT LISTED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is SHENZHEN FIRST UNION TECHNOLOGY CO., LTD.'s FDA import refusal history?

SHENZHEN FIRST UNION TECHNOLOGY CO., LTD. (FEI: 3007522015) has 5 FDA import refusal record(s) in our database, spanning from 12/8/2008 to 5/4/2010.

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 FIRST UNION TECHNOLOGY CO., LTD.'s FEI number is 3007522015.

What types of violations has SHENZHEN FIRST UNION TECHNOLOGY CO., LTD. received?

SHENZHEN FIRST UNION TECHNOLOGY CO., LTD. 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 FIRST UNION TECHNOLOGY CO., LTD. come from?

All FDA import refusal data for SHENZHEN FIRST UNION 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.