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Weisky Technology Co.

⚠️ Moderate Risk

FEI: 3009804541 • Shenzhenshenzhen • CHINA

FEI

FEI Number

3009804541

📍

Location

Shenzhenshenzhen

🇨🇳

Country

CHINA
🏢

Address

4th Floor , Meilong Yuanmeilong Road, , Shenzhenshenzhen, , China

Moderate Risk

FDA Import Risk Assessment

26.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
7/1/2013
Latest Refusal
7/1/2013
Earliest Refusal

Score Breakdown

Violation Severity
56.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

37411×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

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
7/1/2013
90IYNSYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC
118NOT LISTED
16DIRECTIONS
3741FRNMFGREG
476NO REGISTR
508NO 510(K)
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Weisky Technology Co.'s FDA import refusal history?

Weisky Technology Co. (FEI: 3009804541) has 1 FDA import refusal record(s) in our database, spanning from 7/1/2013 to 7/1/2013.

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. Weisky Technology Co.'s FEI number is 3009804541.

What types of violations has Weisky Technology Co. received?

Weisky Technology Co. 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 Weisky Technology Co. come from?

All FDA import refusal data for Weisky Technology Co. 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.