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NANJING VESTA NEW TECH MATERIALS

⚠️ Moderate Risk

FEI: 3034879321 • Nanjing • CHINA

FEI

FEI Number

3034879321

📍

Location

Nanjing

🇨🇳

Country

CHINA
🏢

Address

Room 307 Of Building 5, , Nanjing, , China

Moderate Risk

FDA Import Risk Assessment

42.6
LowModerateHighCritical

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

Statistics

1
Total Refusals
7
Unique Violations
2/27/2025
Latest Refusal
2/27/2025
Earliest Refusal

Score Breakdown

Violation Severity
54.3×40%
Refusal Volume
11.2×30%
Recency
82.6×20%
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).

161×

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.

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.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

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).

3441×

WARNINGS

It appears to lack adequate warning against use in a pathological condition or by children where it may be dangerous to health or against an unsafe dose, method, administering duration, application, in manner/form, to protect users.

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
2/27/2025
80NSCINJECTOR, PEN
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
341REGISTERED
344WARNINGS
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is NANJING VESTA NEW TECH MATERIALS's FDA import refusal history?

NANJING VESTA NEW TECH MATERIALS (FEI: 3034879321) has 1 FDA import refusal record(s) in our database, spanning from 2/27/2025 to 2/27/2025.

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. NANJING VESTA NEW TECH MATERIALS's FEI number is 3034879321.

What types of violations has NANJING VESTA NEW TECH MATERIALS received?

NANJING VESTA NEW TECH MATERIALS has been cited for 7 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 NANJING VESTA NEW TECH MATERIALS come from?

All FDA import refusal data for NANJING VESTA NEW TECH MATERIALS 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.