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F.C. Incorporation

✅ Low Risk

FEI: 3010184976 • Kyunggido • SOUTH KOREA

FEI

FEI Number

3010184976

📍

Location

Kyunggido

🇰🇷
🏢

Address

1314, , Kyunggido, , South Korea

Low Risk

FDA Import Risk Assessment

19.7
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
6
Unique Violations
12/16/2013
Latest Refusal
12/16/2013
Earliest Refusal

Score Breakdown

Violation Severity
38.3×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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).

32601×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

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).

37411×

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.

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
12/16/2013
76EFWTOOTHBRUSH, MANUAL
118NOT LISTED
3260NO ENGLISH
333LACKS FIRM
341REGISTERED
3741FRNMFGREG
508NO 510(K)
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is F.C. Incorporation's FDA import refusal history?

F.C. Incorporation (FEI: 3010184976) has 1 FDA import refusal record(s) in our database, spanning from 12/16/2013 to 12/16/2013.

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. F.C. Incorporation's FEI number is 3010184976.

What types of violations has F.C. Incorporation received?

F.C. Incorporation has been cited for 6 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 F.C. Incorporation come from?

All FDA import refusal data for F.C. Incorporation 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.