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Southern Honey Bee Company, Ltd

FDA import alert and refusal historyHo Chi Minh City, VietnamFEI 3003003345

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Example subjectSouthern Honey Bee Company, Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Southern Honey Bee Company, Ltd has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 18, 2018, was classified NAI (No 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 NAI (No Action Indicated)

Every FDA record for Southern Honey Bee Company, Ltd

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

2018

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

2012

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

Questions about Southern Honey Bee Company, Ltd

Is Southern Honey Bee Company, Ltd on an FDA import alert?
No listing for Southern Honey Bee Company, Ltd 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 Southern Honey Bee Company, Ltd?
No FDA import refusals for Southern Honey Bee Company, Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Southern Honey Bee Company, Ltd last inspected by FDA?
FDA's most recent inspection of Southern Honey Bee Company, Ltd with a final classification is dated September 18, 2018 and was classified NAI (No Action Indicated).
What is Southern Honey Bee Company, Ltd's FEI number?
Southern Honey Bee Company, Ltd's FDA Establishment Identifier (FEI) is 3003003345.

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Example subjectSouthern Honey Bee Company, 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.