Kimnori Co.,Ltd
FDA import alert and refusal historyHongseong, South KoreaFEI 3010620608
Recorded by FDA as KIMNORI CO.,LTD
As of October 25, 2026, Kimnori Co.,Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on April 17, 2018, 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
- Anchovy · LIST INGRE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kimnori Co.,Ltd
3 records, newest first. Each line links to the FDA page it came from.
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.
- 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).
Questions about Kimnori Co.,Ltd
- Is Kimnori Co.,Ltd on an FDA import alert?
- No listing for Kimnori Co.,Ltd appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the South Korea page.
- Has FDA refused shipments from Kimnori Co.,Ltd?
- Yes. FDA refused 3 shipment lines from Kimnori Co.,Ltd on April 17, 2018. The most recent, on April 17, 2018, was anchovy, charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Kimnori Co.,Ltd's shipments?
- The most frequent charges are MFR INSAN (insanitary manufacturing, processing or packing, 3 lines) and LIST INGRE (ingredients not listed, 1 line).
- What is Kimnori Co.,Ltd's FEI number?
- Kimnori Co.,Ltd's FDA Establishment Identifier (FEI) is 3010620608.
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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.