Eudoro Ruiz Garcia
FDA import alert and refusal historyBuenavista, MexicoFEI 3003528106
As of October 26, 2026, Eudoro Ruiz Garcia (Buenavista, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for papaya (papaw) (subtropical and tropical fruit), raw, fresh, ambient; papaya (papaw) (subtropical and tropical fruit), raw, fresh, refrigerated, published by FDA on September 16, 2009, 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 Eudoro Ruiz Garcia
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listPapaya (Papaw) (Subtropical and Tropical Fruit), Raw, Fresh, Ambient; Papaya (Papaw) (Subtropical and Tropical Fruit), Raw, Fresh, RefrigeratedSource
Questions about Eudoro Ruiz Garcia
- Is Eudoro Ruiz Garcia on an FDA import alert?
- Yes. As of October 26, 2026, Eudoro Ruiz Garcia is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for papaya (papaw) (subtropical and tropical fruit), raw, fresh, ambient; papaya (papaw) (subtropical and tropical fruit), raw, fresh, refrigerated; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Eudoro Ruiz Garcia?
- No FDA import refusals for Eudoro Ruiz Garcia appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Eudoro Ruiz Garcia's FEI number?
- Eudoro Ruiz Garcia's FDA Establishment Identifier (FEI) is 3003528106.
- Can shipments from Eudoro Ruiz Garcia still enter the U.S.?
- Shipments of papaya (papaw) (subtropical and tropical fruit), raw, fresh, ambient; papaya (papaw) (subtropical and tropical fruit), raw, fresh, refrigerated from Eudoro Ruiz Garcia 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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