Chaithavee Ltd., Part.
FDA import alert and refusal historySamphanthawong, ThailandFEI 3009678348
Recorded by FDA as CHAITHAVEE LTD., PART.
As of October 26, 2026, Chaithavee Ltd., Part. (Samphanthawong, Thailand) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for golden dried longan, published by FDA on November 17, 2015, 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Chaithavee Ltd., Part.
2 records, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-08red listGolden Dried LonganSource
2013
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Chaithavee Ltd., Part.
- Is Chaithavee Ltd., Part. on an FDA import alert?
- Yes. As of October 26, 2026, Chaithavee Ltd., Part. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for golden dried longan; FDA published the listing on November 17, 2015.
- Has FDA refused shipments from Chaithavee Ltd., Part.?
- No FDA import refusals for Chaithavee Ltd., Part. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Chaithavee Ltd., Part. last inspected by FDA?
- FDA's most recent inspection of Chaithavee Ltd., Part. with a final classification is dated May 30, 2013 and was classified VAI (Voluntary Action Indicated).
- What is Chaithavee Ltd., Part.'s FEI number?
- Chaithavee Ltd., Part.'s FDA Establishment Identifier (FEI) is 3009678348.
- Can shipments from Chaithavee Ltd., Part. still enter the U.S.?
- Shipments of golden dried longan from Chaithavee Ltd., Part. can be detained without physical examination under Import Alert 99-08; 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.