Badaone Co., Ltd.
FDA import alert and refusal historySeongnam-Si, South KoreaFEI 3009910960
As of October 26, 2026, Badaone Co., Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 5 of its shipment lines between May 30, 2019 and December 6, 2019, most often for insanitary manufacturing, processing or packing (MFR INSAN).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Filefish · SALMONELLA
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Badaone Co., Ltd.
6 records, newest first. Each line links to the FDA page it came from.
2022
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2019
- Import refusalRefused, FilefishSALMONELLAEntry ASW-0124838-3Source
- Import refusalRefused, FilefishSALMONELLAEntry ASW-0124838-3Source
- Import refusalRefused, Soup, n.e.c.LIST INGREMFR INSANUSUAL NAMENUTRIT LBLEntry BMI-0051635-2Source
- Import refusalSource
Refused, 2 lines in one entry: Herring; AnchovyFALSEMFR INSANEntry BMI-0050023-2Show 2 linesHide lines
Refusal charges, in plain English
- MFR INSAN3 refused lines
Insanitary manufacturing, processing or packing
The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.
- SALMONELLA2 refused lines
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
- FALSE1 refused line
False or misleading labeling
The labeling appeared to be false or misleading in some particular.
- LIST INGRE1 refused line
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- NUTRIT LBL1 refused line
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- USUAL NAME1 refused line
Common or usual name missing
The label appeared not to show the common or usual name of the food.
Questions about Badaone Co., Ltd.
- Is Badaone Co., Ltd. on an FDA import alert?
- No listing for Badaone Co., Ltd. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Korea page.
- Has FDA refused shipments from Badaone Co., Ltd.?
- Yes. FDA refused 5 shipment lines from Badaone Co., Ltd. between May 30, 2019 and December 6, 2019. The most recent, on December 6, 2019, was filefish, charged as SALMONELLA (salmonella).
- Why did FDA refuse Badaone Co., Ltd.'s shipments?
- The most frequent charges are MFR INSAN (insanitary manufacturing, processing or packing, 3 lines) and SALMONELLA (salmonella, 2 lines).
- When was Badaone Co., Ltd. last inspected by FDA?
- FDA's most recent inspection of Badaone Co., Ltd. with a final classification is dated November 1, 2022 and was classified VAI (Voluntary Action Indicated).
- What is Badaone Co., Ltd.'s FEI number?
- Badaone Co., Ltd.'s FDA Establishment Identifier (FEI) is 3009910960.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.