Julio A. Nunez - ESI/Almacaribe, Inc.
FDA import alert and refusal historySanto Domingo, Dominican RepublicFEI 3002691881
As of October 26, 2026, Julio A. Nunez - ESI/Almacaribe, Inc. (Santo Domingo, Dominican Republic) is on the red list of FDA Import Alert 99-45 (Foods that are or contain an unsafe food additive) for vanilla extract, published by FDA on March 2, 2023, 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 Julio A. Nunez - ESI/Almacaribe, Inc.
1 record, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 99-45red listVanilla extractSource
Questions about Julio A. Nunez - ESI/Almacaribe, Inc.
- Is Julio A. Nunez - ESI/Almacaribe, Inc. on an FDA import alert?
- Yes. As of October 26, 2026, Julio A. Nunez - ESI/Almacaribe, Inc. is on the red list of FDA Import Alert 99-45, “Foods that are or contain an unsafe food additive”, for vanilla extract; FDA published the listing on March 2, 2023.
- Has FDA refused shipments from Julio A. Nunez - ESI/Almacaribe, Inc.?
- No FDA import refusals for Julio A. Nunez - ESI/Almacaribe, Inc. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Julio A. Nunez - ESI/Almacaribe, Inc.'s FEI number?
- Julio A. Nunez - ESI/Almacaribe, Inc.'s FDA Establishment Identifier (FEI) is 3002691881.
- Can shipments from Julio A. Nunez - ESI/Almacaribe, Inc. still enter the U.S.?
- Shipments of vanilla extract from Julio A. Nunez - ESI/Almacaribe, Inc. 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.