Jirapha Bee Farm
FDA import alert and refusal historyMuang, ThailandFEI 3016965300
As of October 26, 2026, Jirapha Bee Farm (Muang, Thailand) is on the red list of FDA Import Alert 99-47 (Foods that appear adulterated for economic gain) for lychee honey, published by FDA on May 2, 2023, and has 3 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-47 · red list
- Last import refusal
- Honey · SUBSTITUTE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Jirapha Bee Farm
4 records, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 99-47red listLychee HoneySource
2021
- Import refusalSource
Refused, 3 lines in one entry: HoneySUBSTITUTEEntry 9LR-1081562-5Show 3 linesHide lines
- Refused, HoneySUBSTITUTEEntry 9LR-1081562-5Source
- Refused, HoneySUBSTITUTEEntry 9LR-1081562-5Source
- Refused, HoneySUBSTITUTEEntry 9LR-1081562-5Source
Refusal charges, in plain English
- SUBSTITUTE3 refused lines
SUBSTITUTE
Questions about Jirapha Bee Farm
- Is Jirapha Bee Farm on an FDA import alert?
- Yes. As of October 26, 2026, Jirapha Bee Farm is on the red list of FDA Import Alert 99-47, “Foods that appear adulterated for economic gain”, for lychee honey; FDA published the listing on May 2, 2023.
- Has FDA refused shipments from Jirapha Bee Farm?
- Yes. FDA refused 3 shipment lines from Jirapha Bee Farm on June 1, 2021. The most recent, on June 1, 2021, was honey, charged as SUBSTITUTE (substitute).
- Why did FDA refuse Jirapha Bee Farm's shipments?
- The most frequent charge is SUBSTITUTE (substitute, 3 lines).
- What is Jirapha Bee Farm's FEI number?
- Jirapha Bee Farm's FDA Establishment Identifier (FEI) is 3016965300.
- Can shipments from Jirapha Bee Farm still enter the U.S.?
- Shipments of lychee honey from Jirapha Bee Farm can be detained without physical examination under Import Alert 99-47; 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.