Peslasa S.A.
FDA import alert and refusal historyGuayaquil, EcuadorFEI 1000273210
As of October 26, 2026, Peslasa S.A. (Guayaquil, Ecuador) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for whole histamine forming fish, published by FDA on January 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 16-120 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Peslasa S.A.
3 records, newest first. Each line links to the FDA page it came from.
2012
- Import alert listingListed on Import Alert 16-120red listWhole Histamine Forming FishSource
2011
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
2010
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Questions about Peslasa S.A.
- Is Peslasa S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Peslasa S.A. is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for whole histamine forming fish; FDA published the listing on January 6, 2012.
- Has FDA refused shipments from Peslasa S.A.?
- No FDA import refusals for Peslasa S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Peslasa S.A. last inspected by FDA?
- FDA's most recent inspection of Peslasa S.A. with a final classification is dated August 16, 2011 and was classified OAI (Official Action Indicated).
- What is Peslasa S.A.'s FEI number?
- Peslasa S.A.'s FDA Establishment Identifier (FEI) is 1000273210.
- Can shipments from Peslasa S.A. still enter the U.S.?
- Shipments of whole histamine forming fish from Peslasa S.A. can be detained without physical examination under Import Alert 16-120; 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.