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DN99 INTERNATIONAL COMPANY LIMITED

⚠️ Moderate Risk

FEI: 3017483450 • Chon Thanh, BINH PHUOC • VIETNAM

FEI

FEI Number

3017483450

📍

Location

Chon Thanh, BINH PHUOC

🇻🇳

Country

VIETNAM
🏢

Address

Lot A3.6 Chon Thanh 1 Industries, , Chon Thanh, BINH PHUOC, Vietnam

Moderate Risk

FDA Import Risk Assessment

34.4
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
9/21/2022
Latest Refusal
9/21/2022
Earliest Refusal

Score Breakdown

Violation Severity
52.3×40%
Refusal Volume
22.3×30%
Recency
18.8×20%
Frequency
30.0×10%
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

2233×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

3413×

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).

5083×

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.

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.

Refusal History

DateProductViolationsDivision
9/21/2022
80LZAGLOVE, PATIENT EXAMINATION, POLY
223FALSE
341REGISTERED
508NO 510(K)
Division of West Coast Imports (DWCI)
9/21/2022
80LZAGLOVE, PATIENT EXAMINATION, POLY
118NOT LISTED
223FALSE
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of West Coast Imports (DWCI)
9/21/2022
80LZAGLOVE, PATIENT EXAMINATION, POLY
118NOT LISTED
223FALSE
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is DN99 INTERNATIONAL COMPANY LIMITED's FDA import refusal history?

DN99 INTERNATIONAL COMPANY LIMITED (FEI: 3017483450) has 3 FDA import refusal record(s) in our database, spanning from 9/21/2022 to 9/21/2022.

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. DN99 INTERNATIONAL COMPANY LIMITED's FEI number is 3017483450.

What types of violations has DN99 INTERNATIONAL COMPANY LIMITED received?

DN99 INTERNATIONAL COMPANY LIMITED 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 DN99 INTERNATIONAL COMPANY LIMITED come from?

All FDA import refusal data for DN99 INTERNATIONAL COMPANY LIMITED 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.