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Beijing ADSS Development Co., Ltd.

⚠️ Moderate Risk

FEI: 3026540836 • Langfang, Hebei • CHINA

FEI

FEI Number

3026540836

📍

Location

Langfang, Hebei

🇨🇳

Country

CHINA
🏢

Address

Southern Area, Fuda Road - Tongsheng Road, Langfang, Hebei, China

Moderate Risk

FDA Import Risk Assessment

42.9
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
5/15/2025
Latest Refusal
2/14/2024
Earliest Refusal

Score Breakdown

Violation Severity
54.0×40%
Refusal Volume
17.7×30%
Recency
71.8×20%
Frequency
16.0×10%
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

4762×

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).

32801×

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.

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).

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
5/15/2025
79GEXPOWERED LASER SURGICAL INSTRUMENTS
341REGISTERED
476NO REGISTR
Division of West Coast Imports (DWCI)
2/14/2024
79OLPOVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE
3280FRNMFGREG
476NO REGISTR
508NO 510(K)
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is Beijing ADSS Development Co., Ltd.'s FDA import refusal history?

Beijing ADSS Development Co., Ltd. (FEI: 3026540836) has 2 FDA import refusal record(s) in our database, spanning from 2/14/2024 to 5/15/2025.

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. Beijing ADSS Development Co., Ltd.'s FEI number is 3026540836.

What types of violations has Beijing ADSS Development Co., Ltd. received?

Beijing ADSS Development 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 Beijing ADSS Development Co., Ltd. come from?

All FDA import refusal data for Beijing ADSS Development 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.