Kingdom Etumax Bio Sdn Bhd
FDA import alert and refusal historyPetaling, MalaysiaFEI 3026093959
Recorded by FDA as KINGDOM ETUMAX BIO SDN BHD
As of October 26, 2026, Kingdom Etumax Bio Sdn Bhd (Petaling, Malaysia) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for kingdom honey royal honey; etumax royal honey, published by FDA on May 2, 2023, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 54-16 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kingdom Etumax Bio Sdn Bhd
1 record, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 54-16red listKingdom Honey Royal Honey; Etumax Royal HoneySource
Questions about Kingdom Etumax Bio Sdn Bhd
- Is Kingdom Etumax Bio Sdn Bhd on an FDA import alert?
- Yes. As of October 26, 2026, Kingdom Etumax Bio Sdn Bhd is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for kingdom honey royal honey; etumax royal honey; FDA published the listing on May 2, 2023.
- Has FDA refused shipments from Kingdom Etumax Bio Sdn Bhd?
- No FDA import refusals for Kingdom Etumax Bio Sdn Bhd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Kingdom Etumax Bio Sdn Bhd's FEI number?
- Kingdom Etumax Bio Sdn Bhd's FDA Establishment Identifier (FEI) is 3026093959.
- Can shipments from Kingdom Etumax Bio Sdn Bhd still enter the U.S.?
- Shipments of kingdom honey royal honey; etumax royal honey from Kingdom Etumax Bio Sdn Bhd can be detained without physical examination under Import Alert 54-16; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.