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AGV Products Corporation

FDA import alert and refusal historyChiayi Hsien, TaiwanFEI 3004253742

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Example subjectAGV Products Corporatio added to Import Alert 16-129 (red list)

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As of October 26, 2026, AGV Products Corporation has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on December 7, 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 AGV Products Corporation

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

2012

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

Questions about AGV Products Corporation

Is AGV Products Corporation on an FDA import alert?
No listing for AGV Products Corporation appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Taiwan page.
Has FDA refused shipments from AGV Products Corporation?
No FDA import refusals for AGV Products Corporation appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was AGV Products Corporation last inspected by FDA?
FDA's most recent inspection of AGV Products Corporation with a final classification is dated December 7, 2017 and was classified VAI (Voluntary Action Indicated).
What is AGV Products Corporation's FEI number?
AGV Products Corporation's FDA Establishment Identifier (FEI) is 3004253742.

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Example subjectAGV Products Corporatio 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.