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Dongnai Honeybee Corporation

FDA import alert and refusal historyBien Hoa, VietnamFEI 3004287484

Recorded by FDA as DONGNAI HONEYBEE CORPORATION

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Example subjectDongnai Honeybee Corporatio added to Import Alert 16-129 (red list)

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As of October 26, 2026, Dongnai Honeybee Corporation has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on June 14, 2023, 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 Dongnai Honeybee Corporation

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

2023

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

2012

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

Questions about Dongnai Honeybee Corporation

Is Dongnai Honeybee Corporation on an FDA import alert?
No listing for Dongnai Honeybee Corporation appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Vietnam page.
Has FDA refused shipments from Dongnai Honeybee Corporation?
No FDA import refusals for Dongnai Honeybee Corporation appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Dongnai Honeybee Corporation last inspected by FDA?
FDA's most recent inspection of Dongnai Honeybee Corporation with a final classification is dated June 14, 2023 and was classified VAI (Voluntary Action Indicated).
What is Dongnai Honeybee Corporation's FEI number?
Dongnai Honeybee Corporation's FDA Establishment Identifier (FEI) is 3004287484.

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Example subjectDongnai Honeybee 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.