Pureco Ojeda, Alberto Y Purecho Caballero Hipolito
FDA import alert and refusal historySanta Clara Del Cobre, MexicoFEI 3009145044
As of October 26, 2026, Pureco Ojeda, Alberto Y Purecho Caballero Hipolito (Santa Clara Del Cobre, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for avocados (hass or hass like), published by FDA on February 26, 2015, 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 99-05 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Pureco Ojeda, Alberto Y Purecho Caballero Hipolito
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-05red listAvocados (Hass or Hass Like)Source
Questions about Pureco Ojeda, Alberto Y Purecho Caballero Hipolito
- Is Pureco Ojeda, Alberto Y Purecho Caballero Hipolito on an FDA import alert?
- Yes. As of October 26, 2026, Pureco Ojeda, Alberto Y Purecho Caballero Hipolito is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for avocados (hass or hass like); FDA published the listing on February 26, 2015.
- Has FDA refused shipments from Pureco Ojeda, Alberto Y Purecho Caballero Hipolito?
- No FDA import refusals for Pureco Ojeda, Alberto Y Purecho Caballero Hipolito appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Pureco Ojeda, Alberto Y Purecho Caballero Hipolito's FEI number?
- Pureco Ojeda, Alberto Y Purecho Caballero Hipolito's FDA Establishment Identifier (FEI) is 3009145044.
- Can shipments from Pureco Ojeda, Alberto Y Purecho Caballero Hipolito still enter the U.S.?
- Shipments of avocados (hass or hass like) from Pureco Ojeda, Alberto Y Purecho Caballero Hipolito can be detained without physical examination under Import Alert 99-05; 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.