Miyaquil SA
FDA import alert and refusal historyGuayaquil, EcuadorFEI 3011288973
Recorded by FDA as MIYAQUIL SA
As of October 26, 2026, Miyaquil SA (Guayaquil, Ecuador) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for frozen pre-cooked clams, published by FDA on September 13, 2019, 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 Miyaquil SA
3 records, newest first. Each line links to the FDA page it came from.
2019
- Import alert listingListed on Import Alert 16-120red listFrozen Pre-Cooked ClamsSource
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
2016
- InspectionInspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Miyaquil SA
- Is Miyaquil SA on an FDA import alert?
- Yes. As of October 26, 2026, Miyaquil SA is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for frozen pre-cooked clams; FDA published the listing on September 13, 2019.
- Has FDA refused shipments from Miyaquil SA?
- No FDA import refusals for Miyaquil SA appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Miyaquil SA last inspected by FDA?
- FDA's most recent inspection of Miyaquil SA with a final classification is dated June 4, 2019 and was classified OAI (Official Action Indicated).
- What is Miyaquil SA's FEI number?
- Miyaquil SA's FDA Establishment Identifier (FEI) is 3011288973.
- Can shipments from Miyaquil SA still enter the U.S.?
- Shipments of frozen pre-cooked clams from Miyaquil SA 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.