Samheung Company
FDA import alert and refusal historyHanam City, South KoreaFEI 3003502078
As of October 26, 2026, Samheung Company (Hanam City, South Korea) is on the red list of FDA Import Alert 99-22 (Undeclared or mislabeled major food allergens) for korean pie (momgchel tongtong), published by FDA on November 9, 2012, is also listed on Import Alert 16-81 (red list) and Import Alert 99-21 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Samheung Company
3 records, newest first. Each line links to the FDA page it came from.
2012
- Import alert listingListed on Import Alert 99-22red listKorean Pie (Momgchel Tongtong)Source
2009
- Import alert listingListed on Import Alert 16-81red listFilefishSource
- Import alert listingListed on Import Alert 99-21red listShrimp & Prawns, Ntrl/Artfcl DriedSource
Questions about Samheung Company
- Is Samheung Company on an FDA import alert?
- Yes. As of October 26, 2026, Samheung Company is on the red list of FDA Import Alert 99-22, “Undeclared or mislabeled major food allergens”, for korean pie (momgchel tongtong); FDA published the listing on November 9, 2012.
- Has FDA refused shipments from Samheung Company?
- No FDA import refusals for Samheung Company appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Samheung Company's FEI number?
- Samheung Company's FDA Establishment Identifier (FEI) is 3003502078.
- Can shipments from Samheung Company still enter the U.S.?
- Shipments of korean pie (momgchel tongtong) from Samheung Company can be detained without physical examination under Import Alert 99-22; 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.