SupplierRadar

Akmal

FDA import alert and refusal historyPontianak, IndonesiaFEI 3018916140

Recorded by FDA as AKMAL

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Example subjectAkma added to Import Alert 16-129 (red list)

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As of October 26, 2026, Akmal is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between June 10, 2021 and July 22, 2021, most often for dietary ingredient without safety assurance (UNSFDIETSP).

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

Current status

Import alerts
Not listed
Last import refusal
Kratom (herbal and botanical teas ii, continued) · UNSFDIETSP
Last warning letter
None found
Last inspection
None on record

Every FDA record for Akmal

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

2021

  1. Import refusal
    Refused, Kratom (herbal and botanical teas ii, continued)UNSFDIETSPEntry SCS-6220493-0
    Source
  2. Import refusal
    Refused, Kratom (herbal and botanical teas ii, continued)UNSFDIETSPEntry SCS-5788169-2
    Source

Refusal charges, in plain English

  • UNSFDIETSP2 refused lines

    Dietary ingredient without safety assurance

    The product appeared to be a dietary supplement or dietary ingredient for which there is inadequate information to provide reasonable assurance that it does not present a significant or unreasonable risk of illness or injury.

Questions about Akmal

Is Akmal on an FDA import alert?
No listing for Akmal appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Indonesia page.
Has FDA refused shipments from Akmal?
Yes. FDA refused 2 shipment lines from Akmal between June 10, 2021 and July 22, 2021. The most recent, on July 22, 2021, was kratom (herbal and botanical teas ii, continued), charged as UNSFDIETSP (dietary ingredient without safety assurance).
Why did FDA refuse Akmal's shipments?
The most frequent charge is UNSFDIETSP (dietary ingredient without safety assurance, 2 lines).
What is Akmal's FEI number?
Akmal's FDA Establishment Identifier (FEI) is 3018916140.

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Example subjectAkma 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.