N. Zeppone & Cia Ltda
FDA import alert and refusal historyJapura, BrazilFEI 3010089051
As of October 26, 2026, N. Zeppone & Cia Ltda is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 28, 2018, 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
- Tamarind (subtropical/tropical fruit pulp) · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for N. Zeppone & Cia Ltda
2 records, newest first. Each line links to the FDA page it came from.
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 N. Zeppone & Cia Ltda
- Is N. Zeppone & Cia Ltda on an FDA import alert?
- No listing for N. Zeppone & Cia Ltda appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Brazil page.
- Has FDA refused shipments from N. Zeppone & Cia Ltda?
- Yes. FDA refused 1 shipment line from N. Zeppone & Cia Ltda on September 28, 2018. The most recent, on September 28, 2018, was tamarind (subtropical/tropical fruit pulp), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse N. Zeppone & Cia Ltda's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- When was N. Zeppone & Cia Ltda last inspected by FDA?
- FDA's most recent inspection of N. Zeppone & Cia Ltda with a final classification is dated March 17, 2015 and was classified VAI (Voluntary Action Indicated).
- What is N. Zeppone & Cia Ltda's FEI number?
- N. Zeppone & Cia Ltda's FDA Establishment Identifier (FEI) is 3010089051.
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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.