The Green Farmer SAC
FDA import alert and refusal historyCallao, PeruFEI 3004272511
As of October 26, 2026, The Green Farmer SAC (Callao, Peru) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for seafood mix, published by FDA on August 25, 2011, is also listed on Import Alert 99-08 (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 16-39 · red listIA 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for The Green Farmer SAC
3 records, newest first. Each line links to the FDA page it came from.
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2011
- Import alert listingListed on Import Alert 16-39red listSeafood MixSource
2009
- Import alert listingListed on Import Alert 99-08red listPanca Pepper PasteSource
Questions about The Green Farmer SAC
- Is The Green Farmer SAC on an FDA import alert?
- Yes. As of October 26, 2026, The Green Farmer SAC is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for seafood mix; FDA published the listing on August 25, 2011.
- Has FDA refused shipments from The Green Farmer SAC?
- No FDA import refusals for The Green Farmer SAC appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was The Green Farmer SAC last inspected by FDA?
- FDA's most recent inspection of The Green Farmer SAC with a final classification is dated March 2, 2016 and was classified VAI (Voluntary Action Indicated).
- What is The Green Farmer SAC's FEI number?
- The Green Farmer SAC's FDA Establishment Identifier (FEI) is 3004272511.
- Can shipments from The Green Farmer SAC still enter the U.S.?
- Shipments of seafood mix from The Green Farmer SAC can be detained without physical examination under Import Alert 16-39; 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.