Incopesca Industria E Comercio De Pesca Do piaui SA
FDA import alert and refusal historyFortaleza, BrazilFEI 13169
As of October 26, 2026, Incopesca Industria E Comercio De Pesca Do piaui SA (Fortaleza, Brazil) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for frozen rock lobster tail; frozen shrimp, 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 Incopesca Industria E Comercio De Pesca Do piaui SA
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-21red listfrozen rock lobster tail; Frozen ShrimpSource
Questions about Incopesca Industria E Comercio De Pesca Do piaui SA
- Is Incopesca Industria E Comercio De Pesca Do piaui SA on an FDA import alert?
- Yes. As of October 26, 2026, Incopesca Industria E Comercio De Pesca Do piaui SA is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for frozen rock lobster tail; frozen shrimp; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Incopesca Industria E Comercio De Pesca Do piaui SA?
- No FDA import refusals for Incopesca Industria E Comercio De Pesca Do piaui SA appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Incopesca Industria E Comercio De Pesca Do piaui SA's FEI number?
- Incopesca Industria E Comercio De Pesca Do piaui SA's FDA Establishment Identifier (FEI) is 13169.
- Can shipments from Incopesca Industria E Comercio De Pesca Do piaui SA still enter the U.S.?
- Shipments of frozen rock lobster tail; frozen shrimp from Incopesca Industria E Comercio De Pesca Do piaui SA 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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