Marco Antonio Garza Arevalo
FDA import alert and refusal historyReynosa, MexicoFEI 3007343776
Recorded by FDA as MARCO ANTONIO GARZA AREVALO
As of October 26, 2026, Marco Antonio Garza Arevalo (Reynosa, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for papayas, published by FDA on November 13, 2009, 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 99-05 · 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 Marco Antonio Garza Arevalo
2 records, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listPapayasSource
- Import alert listingListed on Import Alert 45-02red listGround Morita PepperSource
Questions about Marco Antonio Garza Arevalo
- Is Marco Antonio Garza Arevalo on an FDA import alert?
- Yes. As of October 26, 2026, Marco Antonio Garza Arevalo is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for papayas; FDA published the listing on November 13, 2009.
- Has FDA refused shipments from Marco Antonio Garza Arevalo?
- No FDA import refusals for Marco Antonio Garza Arevalo appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Marco Antonio Garza Arevalo's FEI number?
- Marco Antonio Garza Arevalo's FDA Establishment Identifier (FEI) is 3007343776.
- Can shipments from Marco Antonio Garza Arevalo still enter the U.S.?
- Shipments of papayas from Marco Antonio Garza Arevalo 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.