Sociedad Guidomar Ltda
FDA import alert and refusal historyCoquimbo, ChileFEI 3008845581
As of October 26, 2026, Sociedad Guidomar Ltda (Coquimbo, Chile) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for langostinos, published by FDA on October 28, 2010, 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 list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Sociedad Guidomar Ltda
2 records, newest first. Each line links to the FDA page it came from.
2014
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
2010
- Import alert listingListed on Import Alert 16-39red listLangostinosSource
Questions about Sociedad Guidomar Ltda
- Is Sociedad Guidomar Ltda on an FDA import alert?
- Yes. As of October 26, 2026, Sociedad Guidomar Ltda is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for langostinos; FDA published the listing on October 28, 2010.
- Has FDA refused shipments from Sociedad Guidomar Ltda?
- No FDA import refusals for Sociedad Guidomar Ltda appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Sociedad Guidomar Ltda last inspected by FDA?
- FDA's most recent inspection of Sociedad Guidomar Ltda with a final classification is dated May 23, 2014 and was classified OAI (Official Action Indicated).
- What is Sociedad Guidomar Ltda's FEI number?
- Sociedad Guidomar Ltda's FDA Establishment Identifier (FEI) is 3008845581.
- Can shipments from Sociedad Guidomar Ltda still enter the U.S.?
- Shipments of langostinos from Sociedad Guidomar Ltda 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.