Antarfish Sociedad Anonima
FDA import alert and refusal historySantiago, ChileFEI 1000145352
As of October 26, 2026, Antarfish Sociedad Anonima (Santiago, Chile) is on the red list of FDA Import Alert 16-105 (Fish products: decomposition, histamine or indole) for fresh and frozen; scallops, raw - fresh, frozen, natural state, published by FDA on September 10, 2009, is also listed on Import Alert 16-39 (red list), 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 16-105 · red listIA 16-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Antarfish Sociedad Anonima
2 records, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-105red listfresh and frozen; Scallops, Raw - Fresh, Frozen, Natural StateSource
- Import alert listingListed on Import Alert 16-39red listFrozen Snow Crab MeatSource
Questions about Antarfish Sociedad Anonima
- Is Antarfish Sociedad Anonima on an FDA import alert?
- Yes. As of October 26, 2026, Antarfish Sociedad Anonima is on the red list of FDA Import Alert 16-105, “Fish products: decomposition, histamine or indole”, for fresh and frozen; scallops, raw - fresh, frozen, natural state; FDA published the listing on September 10, 2009.
- Has FDA refused shipments from Antarfish Sociedad Anonima?
- No FDA import refusals for Antarfish Sociedad Anonima appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Antarfish Sociedad Anonima's FEI number?
- Antarfish Sociedad Anonima's FDA Establishment Identifier (FEI) is 1000145352.
- Can shipments from Antarfish Sociedad Anonima still enter the U.S.?
- Shipments of fresh and frozen; scallops, raw - fresh, frozen, natural state from Antarfish Sociedad Anonima can be detained without physical examination under Import Alert 16-105; 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.