Jose Luis Morales
FDA import alert and refusal historyJuarez, MexicoFEI 3004353272
As of October 25, 2026, Jose Luis Morales (Juarez, 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 Jose Luis Morales
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 Jose Luis Morales
- Is Jose Luis Morales on an FDA import alert?
- Yes. As of October 25, 2026, Jose Luis Morales 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 Jose Luis Morales?
- No FDA import refusals for Jose Luis Morales appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Jose Luis Morales's FEI number?
- Jose Luis Morales's FDA Establishment Identifier (FEI) is 3004353272.
- Can shipments from Jose Luis Morales 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 Jose Luis Morales 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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