Faustin Joseph
FDA import alert and refusal historyPort Qu Prince, HaitiFEI 3022454740
Recorded by FDA as FAUSTIN JOSEPH
As of October 26, 2026, Faustin Joseph is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on January 5, 2024, 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
- Mushrooms and other fungi products, whole (button), n.e.c. · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Faustin Joseph
1 record, 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.
- LABELING1 refused line
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
Questions about Faustin Joseph
- Is Faustin Joseph on an FDA import alert?
- No listing for Faustin Joseph appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Haiti page.
- Has FDA refused shipments from Faustin Joseph?
- Yes. FDA refused 1 shipment line from Faustin Joseph on January 5, 2024. The most recent, on January 5, 2024, was mushrooms and other fungi products, whole (button), n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Faustin Joseph's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 1 line) and LABELING (fair packaging and labeling act, 1 line).
- What is Faustin Joseph's FEI number?
- Faustin Joseph's FDA Establishment Identifier (FEI) is 3022454740.
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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.