SupplierRadar

Bidor Kwong Heng Sdn Bhd

FDA import alert and refusal historyBidor, MalaysiaFEI 3013292592

Recorded by FDA as BIDOR KWONG HENG SDN BHD

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Example subjectBidor Kwong Heng Sdn Bh added to Import Alert 16-129 (red list)

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As of October 26, 2026, Bidor Kwong Heng Sdn Bhd has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on December 12, 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 Bidor Kwong Heng Sdn Bhd

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)Foodborne Biological Hazards
    Source

Questions about Bidor Kwong Heng Sdn Bhd

Is Bidor Kwong Heng Sdn Bhd on an FDA import alert?
No listing for Bidor Kwong Heng Sdn Bhd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Malaysia page.
Has FDA refused shipments from Bidor Kwong Heng Sdn Bhd?
No FDA import refusals for Bidor Kwong Heng Sdn Bhd appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Bidor Kwong Heng Sdn Bhd last inspected by FDA?
FDA's most recent inspection of Bidor Kwong Heng Sdn Bhd with a final classification is dated December 12, 2018 and was classified VAI (Voluntary Action Indicated).
What is Bidor Kwong Heng Sdn Bhd's FEI number?
Bidor Kwong Heng Sdn Bhd's FDA Establishment Identifier (FEI) is 3013292592.

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Example subjectBidor Kwong Heng Sdn Bh 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.