Haifen Froid
FDA import alert and refusal historyAgadir, MoroccoFEI 3013178867
Recorded by FDA as HAIFEN FROID
As of October 26, 2026, Haifen Froid is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 4, 2017, most often for false or misleading labeling (FALSE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Fish, n.e.c. · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Haifen Froid
1 record, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Fish, n.e.c.FILTHYFALSEUSUAL NAMEEntry 038-0644857-1Source
Refusal charges, in plain English
- FALSE1 refused line
False or misleading labeling
The labeling appeared to be false or misleading in some particular.
- 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.
- USUAL NAME1 refused line
Common or usual name missing
The label appeared not to show the common or usual name of the food.
Questions about Haifen Froid
- Is Haifen Froid on an FDA import alert?
- No listing for Haifen Froid appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Morocco page.
- Has FDA refused shipments from Haifen Froid?
- Yes. FDA refused 1 shipment line from Haifen Froid on May 4, 2017. The most recent, on May 4, 2017, was fish, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Haifen Froid's shipments?
- The most frequent charges are FALSE (false or misleading labeling, 1 line) and FILTHY (filthy, putrid or decomposed substance, 1 line).
- What is Haifen Froid's FEI number?
- Haifen Froid's FDA Establishment Identifier (FEI) is 3013178867.
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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.