Badaone Co., Ltd.
⚠️ Moderate Risk
FEI: 3009910960 • Seongnam, Gyeonggi • SOUTH KOREA
FEI Number
3009910960
Location
Seongnam, Gyeonggi
Country
SOUTH KOREAAddress
495 Seongnam, Jungwon District, Seongnam, Gyeonggi, South Korea
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
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.
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.
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.
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/6/2019 | 16AGT56FILEFISH | 9SALMONELLA | Division of West Coast Imports (DWCI) |
| 12/5/2019 | 16AGT56FILEFISH | 9SALMONELLA | Division of West Coast Imports (DWCI) |
| 9/27/2019 | 38AGT99SOUP, N.E.C. | Division of West Coast Imports (DWCI) | |
| 5/30/2019 | 16AGT01ANCHOVY | 308MFR INSAN | Division of West Coast Imports (DWCI) |
| 5/30/2019 | 16AGT21HERRING | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is Badaone Co., Ltd.'s FDA import refusal history?
Badaone Co., Ltd. (FEI: 3009910960) has 5 FDA import refusal record(s) in our database, spanning from 5/30/2019 to 12/6/2019.
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. Badaone Co., Ltd.'s FEI number is 3009910960.
What types of violations has Badaone Co., Ltd. received?
Badaone Co., Ltd. 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 Badaone Co., Ltd. come from?
All FDA import refusal data for Badaone 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.