Exofrut S.A.
FDA import alert and refusal historyGuayaquil, EcuadorFEI 3004381732
Recorded by FDA as EXOFRUT S.A.
As of October 26, 2026, Exofrut S.A. (Guayaquil, Ecuador) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for star fruit juice, published by FDA on June 6, 2012, 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 NAI (No Action Indicated)
Every FDA record for Exofrut S.A.
2 records, newest first. Each line links to the FDA page it came from.
2012
- Import alert listingListed on Import Alert 99-08red listStar Fruit JuiceSource
2011
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
Questions about Exofrut S.A.
- Is Exofrut S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Exofrut S.A. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for star fruit juice; FDA published the listing on June 6, 2012.
- Has FDA refused shipments from Exofrut S.A.?
- No FDA import refusals for Exofrut S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Exofrut S.A. last inspected by FDA?
- FDA's most recent inspection of Exofrut S.A. with a final classification is dated November 15, 2011 and was classified NAI (No Action Indicated).
- What is Exofrut S.A.'s FEI number?
- Exofrut S.A.'s FDA Establishment Identifier (FEI) is 3004381732.
- Can shipments from Exofrut S.A. still enter the U.S.?
- Shipments of star fruit juice from Exofrut S.A. 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.