Artesanias El Milagro
FDA import alert and refusal historySan Pablo Huixtepec, MexicoFEI 3013263140
Recorded by FDA as ARTESANIAS EL MILAGRO
As of October 26, 2026, Artesanias El Milagro (San Pablo Huixtepec, Mexico) is on the red list of FDA Import Alert 16-74 (Uneviscerated salt-cured, dried, smoked or fermented fish) for dried charal, published by FDA on July 21, 2014, is also listed on Import Alert 45-02 (red list), 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 16-74 · red listIA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Artesanias El Milagro
2 records, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 16-74red listDried CharalSource
- Import alert listingListed on Import Alert 45-02red listPan BreadSource
Questions about Artesanias El Milagro
- Is Artesanias El Milagro on an FDA import alert?
- Yes. As of October 26, 2026, Artesanias El Milagro is on the red list of FDA Import Alert 16-74, “Uneviscerated salt-cured, dried, smoked or fermented fish”, for dried charal; FDA published the listing on July 21, 2014.
- Has FDA refused shipments from Artesanias El Milagro?
- No FDA import refusals for Artesanias El Milagro appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Artesanias El Milagro's FEI number?
- Artesanias El Milagro's FDA Establishment Identifier (FEI) is 3013263140.
- Can shipments from Artesanias El Milagro still enter the U.S.?
- Shipments of dried charal from Artesanias El Milagro can be detained without physical examination under Import Alert 16-74; 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.