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Samhae Commercial Buan Factory

FDA import alert and refusal historyBuan-Gun, South KoreaFEI 3008350590

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Example subjectSamhae Commercial Buan Factor added to Import Alert 16-129 (red list)

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As of October 26, 2026, Samhae Commercial Buan Factory has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on May 2, 2018, 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 Samhae Commercial Buan Factory

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

2018

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2013

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

Questions about Samhae Commercial Buan Factory

Is Samhae Commercial Buan Factory on an FDA import alert?
No listing for Samhae Commercial Buan Factory 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 Samhae Commercial Buan Factory?
No FDA import refusals for Samhae Commercial Buan Factory appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Samhae Commercial Buan Factory last inspected by FDA?
FDA's most recent inspection of Samhae Commercial Buan Factory with a final classification is dated May 2, 2018 and was classified VAI (Voluntary Action Indicated).
What is Samhae Commercial Buan Factory's FEI number?
Samhae Commercial Buan Factory's FDA Establishment Identifier (FEI) is 3008350590.

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Example subjectSamhae Commercial Buan Factor 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.