K-Max International Co., Ltd.
FDA import alert and refusal historySeoul, South KoreaFEI 3001017044
As of October 26, 2026, K-Max International Co., Ltd. (Seoul, South Korea) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for clams; clams, aquaculture harvested fishery/seafood products, published by FDA on August 19, 2010, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for K-Max International Co., Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2010
- Import alert listingListed on Import Alert 16-81red listClams; Clams, Aquaculture Harvested Fishery/Seafood ProductsSource
Questions about K-Max International Co., Ltd.
- Is K-Max International Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, K-Max International Co., Ltd. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for clams; clams, aquaculture harvested fishery/seafood products; FDA published the listing on August 19, 2010.
- Has FDA refused shipments from K-Max International Co., Ltd.?
- No FDA import refusals for K-Max International Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is K-Max International Co., Ltd.'s FEI number?
- K-Max International Co., Ltd.'s FDA Establishment Identifier (FEI) is 3001017044.
- Can shipments from K-Max International Co., Ltd. still enter the U.S.?
- Shipments of clams; clams, aquaculture harvested fishery/seafood products from K-Max International Co., Ltd. can be detained without physical examination under Import Alert 16-81; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.