Rancho Amelia - Sector 1
FDA import alert and refusal historyAcapetahua, MexicoFEI 3008834209
As of October 26, 2026, Rancho Amelia - Sector 1 (Acapetahua, Mexico) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for papaya, published by FDA on August 1, 2011, 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 99-23 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Rancho Amelia - Sector 1
3 records, newest first. Each line links to the FDA page it came from.
2012
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2011
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
- Import alert listingListed on Import Alert 99-23red listPapayaSource
Questions about Rancho Amelia - Sector 1
- Is Rancho Amelia - Sector 1 on an FDA import alert?
- Yes. As of October 26, 2026, Rancho Amelia - Sector 1 is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for papaya; FDA published the listing on August 1, 2011.
- Has FDA refused shipments from Rancho Amelia - Sector 1?
- No FDA import refusals for Rancho Amelia - Sector 1 appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Rancho Amelia - Sector 1 last inspected by FDA?
- FDA's most recent inspection of Rancho Amelia - Sector 1 with a final classification is dated September 13, 2012 and was classified NAI (No Action Indicated).
- What is Rancho Amelia - Sector 1's FEI number?
- Rancho Amelia - Sector 1's FDA Establishment Identifier (FEI) is 3008834209.
- Can shipments from Rancho Amelia - Sector 1 still enter the U.S.?
- Shipments of papaya from Rancho Amelia - Sector 1 can be detained without physical examination under Import Alert 99-23; 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.