San Marino, S.A. de C.V.
FDA import alert and refusal historyAcajutla, El SalvadorFEI 3004314245
As of October 26, 2026, San Marino, S.A. de C.V. (Acajutla, El Salvador) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for shrimp & prawns; shrimp and prawns, aquaculture harvested fishery/seafood products, published by FDA on September 16, 2009, 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 99-21 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for San Marino, S.A. de C.V.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-21red listShrimp & Prawns; Shrimp and prawns, Aquaculture Harvested Fishery/Seafood ProductsSource
Questions about San Marino, S.A. de C.V.
- Is San Marino, S.A. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, San Marino, S.A. de C.V. is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for shrimp & prawns; shrimp and prawns, aquaculture harvested fishery/seafood products; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from San Marino, S.A. de C.V.?
- No FDA import refusals for San Marino, S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is San Marino, S.A. de C.V.'s FEI number?
- San Marino, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3004314245.
- Can shipments from San Marino, S.A. de C.V. still enter the U.S.?
- Shipments of shrimp & prawns; shrimp and prawns, aquaculture harvested fishery/seafood products from San Marino, S.A. de C.V. can be detained without physical examination under Import Alert 99-21; 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.