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Semo Co., Ltd.

FDA import alert and refusal historyEumseong, South KoreaFEI 3011496222

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Example subjectSemo Co., Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Semo Co., Ltd. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on December 3, 2024, was classified VAI (Voluntary Action Indicated).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Semo Co., Ltd.

3 records, newest first. Each line links to the FDA page it came from.

2024

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2013

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ
    Source

2012

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ
    Source

Questions about Semo Co., Ltd.

Is Semo Co., Ltd. on an FDA import alert?
No listing for Semo 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 Semo Co., Ltd.?
No FDA import refusals for Semo Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Semo Co., Ltd. last inspected by FDA?
FDA's most recent inspection of Semo Co., Ltd. with a final classification is dated December 3, 2024 and was classified VAI (Voluntary Action Indicated).
What is Semo Co., Ltd.'s FEI number?
Semo Co., Ltd.'s FDA Establishment Identifier (FEI) is 3011496222.

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Example subjectSemo Co., Ltd added to Import Alert 16-129 (red list)

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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.