ImportRefusal LogoImportRefusal

Kumho Dental Pharm Co., Ltd.

⚠️ Moderate Risk

FEI: 3018448132 • Seoul, Seoul • SOUTH KOREA

FEI

FEI Number

3018448132

📍

Location

Seoul, Seoul

🇰🇷
🏢

Address

62 Gasan-Ro, Geumcheon, Seoul, Seoul, South Korea

Moderate Risk

FDA Import Risk Assessment

27.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
3/4/2020
Latest Refusal
8/31/2017
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
11.9×10%
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

1183×

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).

32803×

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.

3351×

LACKS N/C

The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
3/4/2020
63RBJ99DENTAL CARIES PROPHYLACTIC N.E.C.
118NOT LISTED
3280FRNMFGREG
Division of West Coast Imports (DWCI)
3/4/2020
63RBJ99DENTAL CARIES PROPHYLACTIC N.E.C.
118NOT LISTED
3280FRNMFGREG
Division of West Coast Imports (DWCI)
8/31/2017
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
335LACKS N/C
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Kumho Dental Pharm Co., Ltd.'s FDA import refusal history?

Kumho Dental Pharm Co., Ltd. (FEI: 3018448132) has 3 FDA import refusal record(s) in our database, spanning from 8/31/2017 to 3/4/2020.

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. Kumho Dental Pharm Co., Ltd.'s FEI number is 3018448132.

What types of violations has Kumho Dental Pharm Co., Ltd. received?

Kumho Dental Pharm Co., Ltd. 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 Kumho Dental Pharm Co., Ltd. come from?

All FDA import refusal data for Kumho Dental Pharm 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.