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Anhui Technology I/E Corp

⚠️ Moderate Risk

FEI: 1000195296 • Hefei • CHINA

FEI

FEI Number

1000195296

📍

Location

Hefei

🇨🇳

Country

CHINA
🏢

Address

327 Changjiang 5-6/F Fuda Bldg, , Hefei, , China

Moderate Risk

FDA Import Risk Assessment

29.2
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
4/18/2008
Latest Refusal
12/3/2002
Earliest Refusal

Score Breakdown

Violation Severity
51.7×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
7.4×10%
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).

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).

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).

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
4/18/2008
79LRRKIT, FIRST AID
118NOT LISTED
341REGISTERED
508NO 510(K)
Los Angeles District Office (LOS-DO)
9/26/2006
76EFWTOOTHBRUSH, MANUAL
118NOT LISTED
Chicago District Office (CHI-DO)
9/26/2006
76MMDTOOTHBRUSH, IONIC, BATTERY-POWERED
118NOT LISTED
Chicago District Office (CHI-DO)
12/3/2002
94V07TV RECEIVER OR PRODUCT CONT. TV RECEIVER, TELEVISION, COMPUTER MONITOR
476NO REGISTR
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Anhui Technology I/E Corp's FDA import refusal history?

Anhui Technology I/E Corp (FEI: 1000195296) has 4 FDA import refusal record(s) in our database, spanning from 12/3/2002 to 4/18/2008.

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. Anhui Technology I/E Corp's FEI number is 1000195296.

What types of violations has Anhui Technology I/E Corp received?

Anhui Technology I/E Corp 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 Anhui Technology I/E Corp come from?

All FDA import refusal data for Anhui Technology I/E Corp 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.