Gandules Inc. S.A.C.
FDA import alert and refusal historyChiclayo, PeruFEI 3004264141
As of October 26, 2026, Gandules Inc. S.A.C. (Chiclayo, Peru) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for quinoa seed, published by FDA on July 28, 2014, 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 99-08 · 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 Gandules Inc. S.A.C.
2 records, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-08red listQuinoa SeedSource
2011
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Gandules Inc. S.A.C.
- Is Gandules Inc. S.A.C. on an FDA import alert?
- Yes. As of October 26, 2026, Gandules Inc. S.A.C. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for quinoa seed; FDA published the listing on July 28, 2014.
- Has FDA refused shipments from Gandules Inc. S.A.C.?
- No FDA import refusals for Gandules Inc. S.A.C. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Gandules Inc. S.A.C. last inspected by FDA?
- FDA's most recent inspection of Gandules Inc. S.A.C. with a final classification is dated February 4, 2011 and was classified VAI (Voluntary Action Indicated).
- What is Gandules Inc. S.A.C.'s FEI number?
- Gandules Inc. S.A.C.'s FDA Establishment Identifier (FEI) is 3004264141.
- Can shipments from Gandules Inc. S.A.C. still enter the U.S.?
- Shipments of quinoa seed from Gandules Inc. S.A.C. can be detained without physical examination under Import Alert 99-08; 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.