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Agricola Olivar Felipe Mi

FDA import alert and refusal historyCachapoal, ChileFEI 3011390054

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Example subjectAgricola Olivar Felipe M added to Import Alert 16-129 (red list)

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As of October 26, 2026, Agricola Olivar Felipe Mi (Cachapoal, Chile) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh nectarines; fresh peaches, published by FDA on April 6, 2015, 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 Agricola Olivar Felipe Mi

1 record, newest first. Each line links to the FDA page it came from.

2015

  1. Import alert listing
    Listed on Import Alert 99-05red listFresh Nectarines; Fresh Peaches
    Source

Questions about Agricola Olivar Felipe Mi

Is Agricola Olivar Felipe Mi on an FDA import alert?
Yes. As of October 26, 2026, Agricola Olivar Felipe Mi is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh nectarines; fresh peaches; FDA published the listing on April 6, 2015.
Has FDA refused shipments from Agricola Olivar Felipe Mi?
No FDA import refusals for Agricola Olivar Felipe Mi appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Agricola Olivar Felipe Mi's FEI number?
Agricola Olivar Felipe Mi's FDA Establishment Identifier (FEI) is 3011390054.
Can shipments from Agricola Olivar Felipe Mi still enter the U.S.?
Shipments of fresh nectarines; fresh peaches from Agricola Olivar Felipe Mi 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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Example subjectAgricola Olivar Felipe M added to Import Alert 16-129 (red list)

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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.