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Asl Oharma Sdn Bhd

FDA import alert and refusal historyKuala Lumpur, MalaysiaFEI 3038439103

Recorded by FDA as ASL OHARMA SDN BHD

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Example subjectAsl Oharma Sdn Bh added to Import Alert 16-129 (red list)

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As of October 26, 2026, Asl Oharma Sdn Bhd is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on July 28, 2025, most often for unapproved new drug (UNAPPROVED).

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

Current status

Import alerts
Not listed
Last import refusal
L-tryptophan (protein) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Asl Oharma Sdn Bhd

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

2025

  1. Import refusal
    Refused, L-tryptophan (protein)UNAPPROVEDEntry 799-8899626-1
    Source

Refusal charges, in plain English

  • UNAPPROVED1 refused line

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Asl Oharma Sdn Bhd

Is Asl Oharma Sdn Bhd on an FDA import alert?
No listing for Asl Oharma 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 Asl Oharma Sdn Bhd?
Yes. FDA refused 1 shipment line from Asl Oharma Sdn Bhd on July 28, 2025. The most recent, on July 28, 2025, was l-tryptophan (protein), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Asl Oharma Sdn Bhd's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Asl Oharma Sdn Bhd's FEI number?
Asl Oharma Sdn Bhd's FDA Establishment Identifier (FEI) is 3038439103.

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Example subjectAsl Oharma 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.