Litofish, Lda
FDA import alert and refusal historyFigueira Da Foz, PortugalFEI 3008587406
Recorded by FDA as LITOFISH, LDA
As of October 25, 2026, Litofish, Lda is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 28, 2019, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Cuttlefish, other aquatic species · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Litofish, Lda
3 records, newest first. Each line links to the FDA page it came from.
2019
2014
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Refusal charges, in plain English
- FILTHY1 refused line
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Litofish, Lda
- Is Litofish, Lda on an FDA import alert?
- No listing for Litofish, Lda appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Portugal page.
- Has FDA refused shipments from Litofish, Lda?
- Yes. FDA refused 1 shipment line from Litofish, Lda on May 28, 2019. The most recent, on May 28, 2019, was cuttlefish, other aquatic species, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Litofish, Lda's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- When was Litofish, Lda last inspected by FDA?
- FDA's most recent inspection of Litofish, Lda with a final classification is dated July 19, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Litofish, Lda's FEI number?
- Litofish, Lda's FDA Establishment Identifier (FEI) is 3008587406.
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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.