Roberto Madrid Padilla
FDA import alert and refusal historyTijuana, MexicoFEI 2000045989
Recorded by FDA as ROBERTO MADRID PADILLA
As of October 25, 2026, Roberto Madrid Padilla (Tijuana, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for papaya, published by FDA on September 28, 2011, is also listed on Import Alert 21-17 (green list) and Import Alert 99-23 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Roberto Madrid Padilla
3 records, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 21-17green listPapayaSource
2011
- Import alert listingListed on Import Alert 99-05red listPapayaSource
- Import alert listingListed on Import Alert 99-23red listPapayaSource
Questions about Roberto Madrid Padilla
- Is Roberto Madrid Padilla on an FDA import alert?
- Yes. As of October 25, 2026, Roberto Madrid Padilla is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for papaya; FDA published the listing on September 28, 2011.
- Has FDA refused shipments from Roberto Madrid Padilla?
- No FDA import refusals for Roberto Madrid Padilla appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Roberto Madrid Padilla's FEI number?
- Roberto Madrid Padilla's FDA Establishment Identifier (FEI) is 2000045989.
- Can shipments from Roberto Madrid Padilla still enter the U.S.?
- Shipments of papaya from Roberto Madrid Padilla 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.