L.P. Uyttenwaal B.V.
FDA import alert and refusal historyTer Aar, NetherlandsFEI 3001297674
As of October 26, 2026, L.P. Uyttenwaal B.V. (Ter Aar, Netherlands) is on the red list of FDA Import Alert 99-36 (Low-acid canned/acidified foods: process information) for silverskin onions in sweet vinegar; silverskin onions; coloured with tartrazine e 102 (amsterdam onions); silverskin onions in vinegar solution, published by FDA on June 3, 2014, 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 99-36 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for L.P. Uyttenwaal B.V.
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-36red listSilverskin onions in sweet vinegar; silverskin onions; coloured with tartrazine e 102 (amsterdam onions); silverskin onions in vinegar solutionSource
Questions about L.P. Uyttenwaal B.V.
- Is L.P. Uyttenwaal B.V. on an FDA import alert?
- Yes. As of October 26, 2026, L.P. Uyttenwaal B.V. is on the red list of FDA Import Alert 99-36, “Low-acid canned/acidified foods: process information”, for silverskin onions in sweet vinegar; silverskin onions; coloured with tartrazine e 102 (amsterdam onions); silverskin onions in vinegar solution; FDA published the listing on June 3, 2014.
- Has FDA refused shipments from L.P. Uyttenwaal B.V.?
- No FDA import refusals for L.P. Uyttenwaal B.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is L.P. Uyttenwaal B.V.'s FEI number?
- L.P. Uyttenwaal B.V.'s FDA Establishment Identifier (FEI) is 3001297674.
- Can shipments from L.P. Uyttenwaal B.V. still enter the U.S.?
- Shipments of silverskin onions in sweet vinegar; silverskin onions; coloured with tartrazine e 102 (amsterdam onions); silverskin onions in vinegar solution from L.P. Uyttenwaal B.V. can be detained without physical examination under Import Alert 99-36; 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.