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SHENZHEN SIFIER TECHNOLOGY CO.,

⚠️ Moderate Risk

FEI: 3012818301 • Shenzhen • CHINA

FEI

FEI Number

3012818301

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

Rm 321-322, 3rd Fl, Com, Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

40.0
LowModerateHighCritical

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

Statistics

2
Total Refusals
5
Unique Violations
2/24/2025
Latest Refusal
10/19/2021
Earliest Refusal

Score Breakdown

Violation Severity
51.7×40%
Refusal Volume
17.7×30%
Recency
67.0×20%
Frequency
6.0×10%
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

32802×

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.

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.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

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
2/24/2025
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
3280FRNMFGREG
Division of Southeast Imports (DSEI)
10/19/2021
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SHENZHEN SIFIER TECHNOLOGY CO.,'s FDA import refusal history?

SHENZHEN SIFIER TECHNOLOGY CO., (FEI: 3012818301) has 2 FDA import refusal record(s) in our database, spanning from 10/19/2021 to 2/24/2025.

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 SIFIER TECHNOLOGY CO.,'s FEI number is 3012818301.

What types of violations has SHENZHEN SIFIER TECHNOLOGY CO., received?

SHENZHEN SIFIER 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 SHENZHEN SIFIER TECHNOLOGY CO., come from?

All FDA import refusal data for SHENZHEN SIFIER 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.