Tercon-Sociedade Maritima E De Conservas Terceirence Lda
FDA import alert and refusal historyAngra Do Heroismo, PortugalFEI 10857
As of October 26, 2026, Tercon-Sociedade Maritima E De Conservas Terceirence Lda (Angra Do Heroismo, Portugal) is on the red list of FDA Import Alert 99-36 (Low-acid canned/acidified foods: process information) for tuna in brine, published by FDA on June 3, 2014, 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 99-36 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Tercon-Sociedade Maritima E De Conservas Terceirence Lda
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-36red listTuna in brineSource
Questions about Tercon-Sociedade Maritima E De Conservas Terceirence Lda
- Is Tercon-Sociedade Maritima E De Conservas Terceirence Lda on an FDA import alert?
- Yes. As of October 26, 2026, Tercon-Sociedade Maritima E De Conservas Terceirence Lda is on the red list of FDA Import Alert 99-36, “Low-acid canned/acidified foods: process information”, for tuna in brine; FDA published the listing on June 3, 2014.
- Has FDA refused shipments from Tercon-Sociedade Maritima E De Conservas Terceirence Lda?
- No FDA import refusals for Tercon-Sociedade Maritima E De Conservas Terceirence Lda appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Tercon-Sociedade Maritima E De Conservas Terceirence Lda's FEI number?
- Tercon-Sociedade Maritima E De Conservas Terceirence Lda's FDA Establishment Identifier (FEI) is 10857.
- Can shipments from Tercon-Sociedade Maritima E De Conservas Terceirence Lda still enter the U.S.?
- Shipments of tuna in brine from Tercon-Sociedade Maritima E De Conservas Terceirence Lda can be detained without physical examination under Import Alert 99-36; 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.