KG Lab Co., Ltd.
FDA import alert and refusal historyYangpyeong, South KoreaFEI 3010187101
As of October 25, 2026, KG Lab Co., Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 27, 2025, most often for ingredients not listed (LIST INGRE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Ginseng, juice or drink (root & tuber vegetable) · LIST INGRE
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for KG Lab Co., Ltd.
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Ginseng, juice or drink (root & tuber vegetable)LIST INGRENO PROCESSEntry U47-2500688-4Source
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Refusal charges, in plain English
- 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).
- NO PROCESS1 refused line
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
Questions about KG Lab Co., Ltd.
- Is KG Lab Co., Ltd. on an FDA import alert?
- No listing for KG Lab 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 KG Lab Co., Ltd.?
- Yes. FDA refused 1 shipment line from KG Lab Co., Ltd. on March 27, 2025. The most recent, on March 27, 2025, was ginseng, juice or drink (root & tuber vegetable), charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse KG Lab Co., Ltd.'s shipments?
- The most frequent charges are LIST INGRE (ingredients not listed, 1 line) and NO PROCESS (no scheduled process filed, 1 line).
- When was KG Lab Co., Ltd. last inspected by FDA?
- FDA's most recent inspection of KG Lab Co., Ltd. with a final classification is dated May 24, 2016 and was classified VAI (Voluntary Action Indicated).
- What is KG Lab Co., Ltd.'s FEI number?
- KG Lab Co., Ltd.'s FDA Establishment Identifier (FEI) is 3010187101.
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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.