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SHANGHAI XIANGSHANG CO.,LTD

⚠️ Moderate Risk

FEI: 3016974522 • Jiading • CHINA

FEI

FEI Number

3016974522

📍

Location

Jiading

🇨🇳

Country

CHINA
🏢

Address

(Spb-A)(N3p)No.177 Lane, , Jiading, , China

Moderate Risk

FDA Import Risk Assessment

29.0
LowModerateHighCritical

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

Statistics

2
Total Refusals
5
Unique Violations
3/15/2021
Latest Refusal
11/6/2020
Earliest Refusal

Score Breakdown

Violation Severity
54.3×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

1182×

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).

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.

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).

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
3/15/2021
73PGJOXIMETER, WELLNESS
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
11/6/2020
84GXCDEVICE, ELECTROCONVULSIVE THERAPY
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SHANGHAI XIANGSHANG CO.,LTD's FDA import refusal history?

SHANGHAI XIANGSHANG CO.,LTD (FEI: 3016974522) has 2 FDA import refusal record(s) in our database, spanning from 11/6/2020 to 3/15/2021.

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. SHANGHAI XIANGSHANG CO.,LTD's FEI number is 3016974522.

What types of violations has SHANGHAI XIANGSHANG CO.,LTD received?

SHANGHAI XIANGSHANG CO.,LTD 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 SHANGHAI XIANGSHANG CO.,LTD come from?

All FDA import refusal data for SHANGHAI XIANGSHANG 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.