Kee Wee Hup Kee Manufacture PTE Ltd
FDA import alert and refusal historySingapore, SingaporeFEI 12879
As of October 26, 2026, Kee Wee Hup Kee Manufacture PTE Ltd (Singapore, Singapore) is on the red list of FDA Import Alert 99-45 (Foods that are or contain an unsafe food additive) for all dried preserved fruits, published by FDA on May 12, 2025, 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 99-45 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kee Wee Hup Kee Manufacture PTE Ltd
1 record, newest first. Each line links to the FDA page it came from.
2025
- Import alert listingListed on Import Alert 99-45red listAll Dried Preserved FruitsSource
Questions about Kee Wee Hup Kee Manufacture PTE Ltd
- Is Kee Wee Hup Kee Manufacture PTE Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Kee Wee Hup Kee Manufacture PTE Ltd is on the red list of FDA Import Alert 99-45, “Foods that are or contain an unsafe food additive”, for all dried preserved fruits; FDA published the listing on May 12, 2025.
- Has FDA refused shipments from Kee Wee Hup Kee Manufacture PTE Ltd?
- No FDA import refusals for Kee Wee Hup Kee Manufacture PTE Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Kee Wee Hup Kee Manufacture PTE Ltd's FEI number?
- Kee Wee Hup Kee Manufacture PTE Ltd's FDA Establishment Identifier (FEI) is 12879.
- Can shipments from Kee Wee Hup Kee Manufacture PTE Ltd still enter the U.S.?
- Shipments of all dried preserved fruits from Kee Wee Hup Kee Manufacture PTE Ltd can be detained without physical examination under Import Alert 99-45; 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.