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VIVA CONCEPT TECHNOLOGY CO

⚠️ Moderate Risk

FEI: 3020473940 • Nanjing • CHINA

FEI

FEI Number

3020473940

📍

Location

Nanjing

🇨🇳

Country

CHINA
🏢

Address

Room 3501, Building Pudo, Nanjing, , China

Moderate Risk

FDA Import Risk Assessment

28.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
10/27/2021
Latest Refusal
10/27/2021
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
1.8×20%
Frequency
10.0×10%
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

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).

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.

471×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

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
10/27/2021
95REDLASER ADVERTISING DISPLAY SYSTEM
118NOT LISTED
3280FRNMFGREG
47NON STD
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is VIVA CONCEPT TECHNOLOGY CO's FDA import refusal history?

VIVA CONCEPT TECHNOLOGY CO (FEI: 3020473940) has 1 FDA import refusal record(s) in our database, spanning from 10/27/2021 to 10/27/2021.

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. VIVA CONCEPT TECHNOLOGY CO's FEI number is 3020473940.

What types of violations has VIVA CONCEPT TECHNOLOGY CO received?

VIVA CONCEPT TECHNOLOGY CO 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 VIVA CONCEPT TECHNOLOGY CO come from?

All FDA import refusal data for VIVA CONCEPT 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.