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Aramex (Malaysia) Sdn Bhd

FDA import alert and refusal historyPetaling Jaya, MalaysiaFEI 3009903792

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Example subjectAramex (Malaysia) Sdn Bh added to Import Alert 16-129 (red list)

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As of October 26, 2026, Aramex (Malaysia) Sdn Bhd is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 9, 2019, most often for fair packaging and labeling act (LABELING).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Honey, n.e.c. · LABELING
Last warning letter
None found
Last inspection
None on record

Every FDA record for Aramex (Malaysia) Sdn Bhd

1 record, newest first. Each line links to the FDA page it came from.

2019

  1. Import refusal
    Refused, Honey, n.e.c.LABELINGEntry SCS-6670771-3
    Source

Refusal charges, in plain English

  • LABELING1 refused line

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

Questions about Aramex (Malaysia) Sdn Bhd

Is Aramex (Malaysia) Sdn Bhd on an FDA import alert?
No listing for Aramex (Malaysia) 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 Aramex (Malaysia) Sdn Bhd?
Yes. FDA refused 1 shipment line from Aramex (Malaysia) Sdn Bhd on October 9, 2019. The most recent, on October 9, 2019, was honey, n.e.c., charged as LABELING (fair packaging and labeling act).
Why did FDA refuse Aramex (Malaysia) Sdn Bhd's shipments?
The most frequent charge is LABELING (fair packaging and labeling act, 1 line).
What is Aramex (Malaysia) Sdn Bhd's FEI number?
Aramex (Malaysia) Sdn Bhd's FDA Establishment Identifier (FEI) is 3009903792.

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Example subjectAramex (Malaysia) 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.