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Guilin Sanzhen Foods Co., Ltd

FDA import alert and refusal historyGuilin, ChinaFEI 3007785043

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Example subjectGuilin Sanzhen Foods Co., Lt added to Import Alert 16-129 (red list)

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As of October 27, 2026, Guilin Sanzhen Foods Co., Ltd has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on March 22, 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 Guilin Sanzhen Foods Co., Ltd

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

Questions about Guilin Sanzhen Foods Co., Ltd

Is Guilin Sanzhen Foods Co., Ltd on an FDA import alert?
No listing for Guilin Sanzhen Foods Co., Ltd appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the China page.
Has FDA refused shipments from Guilin Sanzhen Foods Co., Ltd?
No FDA import refusals for Guilin Sanzhen Foods Co., Ltd appear in FDA's refusal data since October 2016, as of October 27, 2026.
When was Guilin Sanzhen Foods Co., Ltd last inspected by FDA?
FDA's most recent inspection of Guilin Sanzhen Foods Co., Ltd with a final classification is dated March 22, 2018 and was classified VAI (Voluntary Action Indicated).
What is Guilin Sanzhen Foods Co., Ltd's FEI number?
Guilin Sanzhen Foods Co., Ltd's FDA Establishment Identifier (FEI) is 3007785043.

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Example subjectGuilin Sanzhen Foods 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.