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STC Nara Co., Ltd

✅ Low Risk

FEI: 3016790229 • Cheonan, Chungcheongnam • SOUTH KOREA

FEI

FEI Number

3016790229

📍

Location

Cheonan, Chungcheongnam

🇰🇷
🏢

Address

Cheonan, 139-11 Mojeon1-Gil; Seobuk, Cheonan, Chungcheongnam, South Korea

Low Risk

FDA Import Risk Assessment

24.4
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
11/13/2006
Latest Refusal
2/9/2005
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
17.1×10%
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

2182×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

3212×

LACKS N/C

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

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).

2601×

FALSE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

3281×

USUAL NAME

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

Refusal History

DateProductViolationsDivision
11/13/2006
66VBR99MISCELLANEOUS PATENT MEDICINES, ETC.
218LIST INGRE
321LACKS N/C
328USUAL NAME
Los Angeles District Office (LOS-DO)
11/13/2006
66VBA99MISCELLANEOUS PATENT MEDICINES, ETC.
218LIST INGRE
260FALSE
321LACKS N/C
Los Angeles District Office (LOS-DO)
2/9/2005
66VCR99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is STC Nara Co., Ltd's FDA import refusal history?

STC Nara Co., Ltd (FEI: 3016790229) has 3 FDA import refusal record(s) in our database, spanning from 2/9/2005 to 11/13/2006.

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. STC Nara Co., Ltd's FEI number is 3016790229.

What types of violations has STC Nara Co., Ltd received?

STC Nara 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 STC Nara Co., Ltd come from?

All FDA import refusal data for STC Nara 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.