Especias Aviles S A De C Vjesus Garcia No 105 Entre
FDA import alert and refusal historyHermosillo, MexicoFEI 1000318742
As of October 26, 2026, Especias Aviles S A De C Vjesus Garcia No 105 Entre (Hermosillo, Mexico) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for mexican style cocoa, published by FDA on April 28, 2017, 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 99-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Especias Aviles S A De C Vjesus Garcia No 105 Entre
1 record, newest first. Each line links to the FDA page it came from.
2017
- Import alert listingListed on Import Alert 99-39red listMexican Style CocoaSource
Questions about Especias Aviles S A De C Vjesus Garcia No 105 Entre
- Is Especias Aviles S A De C Vjesus Garcia No 105 Entre on an FDA import alert?
- Yes. As of October 26, 2026, Especias Aviles S A De C Vjesus Garcia No 105 Entre is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for mexican style cocoa; FDA published the listing on April 28, 2017.
- Has FDA refused shipments from Especias Aviles S A De C Vjesus Garcia No 105 Entre?
- No FDA import refusals for Especias Aviles S A De C Vjesus Garcia No 105 Entre appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Especias Aviles S A De C Vjesus Garcia No 105 Entre's FEI number?
- Especias Aviles S A De C Vjesus Garcia No 105 Entre's FDA Establishment Identifier (FEI) is 1000318742.
- Can shipments from Especias Aviles S A De C Vjesus Garcia No 105 Entre still enter the U.S.?
- Shipments of mexican style cocoa from Especias Aviles S A De C Vjesus Garcia No 105 Entre can be detained without physical examination under Import Alert 99-39; 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.