Boonmee International Co.
FDA import alert and refusal historyPathumtani, ThailandFEI 3001916127
As of October 26, 2026, Boonmee International Co. (Pathumtani, Thailand) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for durian, durion (subtropical and tropical fruit), raw - fresh, frozen, natural state, published by FDA on September 16, 2009, 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
- None on record
Every FDA record for Boonmee International Co.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-08red listDurian, Durion (Subtropical and Tropical Fruit), Raw - Fresh, Frozen, Natural StateSource
Questions about Boonmee International Co.
- Is Boonmee International Co. on an FDA import alert?
- Yes. As of October 26, 2026, Boonmee International Co. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for durian, durion (subtropical and tropical fruit), raw - fresh, frozen, natural state; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Boonmee International Co.?
- No FDA import refusals for Boonmee International Co. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Boonmee International Co.'s FEI number?
- Boonmee International Co.'s FDA Establishment Identifier (FEI) is 3001916127.
- Can shipments from Boonmee International Co. still enter the U.S.?
- Shipments of durian, durion (subtropical and tropical fruit), raw - fresh, frozen, natural state from Boonmee International Co. 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.