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Hyosong Green Food Co Ltd

FDA import alert and refusal historyGunsan, South KoreaFEI 3009302299

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Example subjectHyosong Green Food Co Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Hyosong Green Food Co Ltd has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on August 24, 2017, 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 Hyosong Green Food Co Ltd

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

2017

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

2013

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

Questions about Hyosong Green Food Co Ltd

Is Hyosong Green Food Co Ltd on an FDA import alert?
No listing for Hyosong Green Food 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 Hyosong Green Food Co Ltd?
No FDA import refusals for Hyosong Green Food Co Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Hyosong Green Food Co Ltd last inspected by FDA?
FDA's most recent inspection of Hyosong Green Food Co Ltd with a final classification is dated August 24, 2017 and was classified VAI (Voluntary Action Indicated).
What is Hyosong Green Food Co Ltd's FEI number?
Hyosong Green Food Co Ltd's FDA Establishment Identifier (FEI) is 3009302299.

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Example subjectHyosong Green Food Co Lt 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.