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Oversea Production Sdn. Bhd.

FDA import alert and refusal historyShah Alam, MalaysiaFEI 3004347759

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Example subjectOversea Production Sdn. Bhd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Oversea Production Sdn. Bhd. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on May 16, 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 Oversea Production Sdn. Bhd.

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)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Questions about Oversea Production Sdn. Bhd.

Is Oversea Production Sdn. Bhd. on an FDA import alert?
No listing for Oversea Production 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 Oversea Production Sdn. Bhd.?
No FDA import refusals for Oversea Production Sdn. Bhd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Oversea Production Sdn. Bhd. last inspected by FDA?
FDA's most recent inspection of Oversea Production Sdn. Bhd. with a final classification is dated May 16, 2023 and was classified VAI (Voluntary Action Indicated).
What is Oversea Production Sdn. Bhd.'s FEI number?
Oversea Production Sdn. Bhd.'s FDA Establishment Identifier (FEI) is 3004347759.

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Example subjectOversea Production Sdn. Bhd 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.