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SHANGHAIHUACHEN MEDICAL INSTRUMENTS CO., LTD

⚠️ Moderate Risk

FEI: 3008303451 • Shanghai, Shanghai • CHINA

FEI

FEI Number

3008303451

📍

Location

Shanghai, Shanghai

🇨🇳

Country

CHINA
🏢

Address

# 2723 Taihe West Rd, , Shanghai, Shanghai, China

Moderate Risk

FDA Import Risk Assessment

35.7
LowModerateHighCritical

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

Statistics

11
Total Refusals
3
Unique Violations
10/17/2016
Latest Refusal
5/27/2013
Earliest Refusal

Score Breakdown

Violation Severity
51.2×40%
Refusal Volume
40.0×30%
Recency
0.0×20%
Frequency
32.4×10%
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

11810×

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).

32806×

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.

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
10/17/2016
80FLKTHERMOMETER, CLINICAL MERCURY
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
9/18/2015
80FLKTHERMOMETER, CLINICAL MERCURY
118NOT LISTED
Division of Southeast Imports (DSEI)
9/14/2015
80FLKTHERMOMETER, CLINICAL MERCURY
118NOT LISTED
Division of Southeast Imports (DSEI)
6/26/2015
80FLKTHERMOMETER, CLINICAL MERCURY
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
8/15/2014
80FLKTHERMOMETER, CLINICAL MERCURY
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
7/9/2014
80FLKTHERMOMETER, CLINICAL MERCURY
118NOT LISTED
Division of Southeast Imports (DSEI)
3/18/2014
80FLKTHERMOMETER, CLINICAL MERCURY
3280FRNMFGREG
Division of Southeast Imports (DSEI)
2/19/2014
80FLKTHERMOMETER, CLINICAL MERCURY
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
10/23/2013
80FLKTHERMOMETER, CLINICAL MERCURY
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
6/25/2013
80FLKTHERMOMETER, CLINICAL MERCURY
118NOT LISTED
508NO 510(K)
Florida District Office (FLA-DO)
5/27/2013
80FLKTHERMOMETER, CLINICAL MERCURY
118NOT LISTED
Florida District Office (FLA-DO)

Frequently Asked Questions

What is SHANGHAIHUACHEN MEDICAL INSTRUMENTS CO., LTD's FDA import refusal history?

SHANGHAIHUACHEN MEDICAL INSTRUMENTS CO., LTD (FEI: 3008303451) has 11 FDA import refusal record(s) in our database, spanning from 5/27/2013 to 10/17/2016.

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. SHANGHAIHUACHEN MEDICAL INSTRUMENTS CO., LTD's FEI number is 3008303451.

What types of violations has SHANGHAIHUACHEN MEDICAL INSTRUMENTS CO., LTD received?

SHANGHAIHUACHEN MEDICAL INSTRUMENTS CO., LTD has been cited for 3 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 SHANGHAIHUACHEN MEDICAL INSTRUMENTS CO., LTD come from?

All FDA import refusal data for SHANGHAIHUACHEN MEDICAL INSTRUMENTS 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.