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Greatsun Industrial Co Ltd

⚠️ Moderate Risk

FEI: 3006095264 • Shenzhenshenzhen • CHINA

FEI

FEI Number

3006095264

📍

Location

Shenzhenshenzhen

🇨🇳

Country

CHINA
🏢

Address

Flat B 3/F No 271long Shan Xin Chunlong, , Shenzhenshenzhen, , China

Moderate Risk

FDA Import Risk Assessment

39.7
LowModerateHighCritical

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

Statistics

7
Total Refusals
4
Unique Violations
7/23/2013
Latest Refusal
5/31/2013
Earliest Refusal

Score Breakdown

Violation Severity
56.7×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
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

166×

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.

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.

37412×

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.

Refusal History

DateProductViolationsDivision
7/23/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
New York District Office (NYK-DO)
7/23/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
3741FRNMFGREG
New York District Office (NYK-DO)
5/31/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
16DIRECTIONS
New York District Office (NYK-DO)
5/31/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
16DIRECTIONS
New York District Office (NYK-DO)
5/31/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
16DIRECTIONS
New York District Office (NYK-DO)
5/31/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
16DIRECTIONS
New York District Office (NYK-DO)
5/31/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
16DIRECTIONS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Greatsun Industrial Co Ltd's FDA import refusal history?

Greatsun Industrial Co Ltd (FEI: 3006095264) has 7 FDA import refusal record(s) in our database, spanning from 5/31/2013 to 7/23/2013.

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. Greatsun Industrial Co Ltd's FEI number is 3006095264.

What types of violations has Greatsun Industrial Co Ltd received?

Greatsun Industrial 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 Greatsun Industrial Co Ltd come from?

All FDA import refusal data for Greatsun Industrial 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.