Kenscoff Manufacturing
FDA import alert and refusal historyPort Au Prince, HaitiFEI 3010818478
As of October 26, 2026, Kenscoff Manufacturing is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on January 16, 2024, most often for ingredients not listed (LIST INGRE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- African spinach, dried or paste · LIST INGRE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kenscoff Manufacturing
1 record, newest first. Each line links to the FDA page it came from.
2024
- Import refusalRefused, African spinach, dried or pasteLIST INGRENUTRIT LBLEntry FX6-0101643-8Source
Refusal charges, in plain English
- LIST INGRE1 refused line
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- NUTRIT LBL1 refused line
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
Questions about Kenscoff Manufacturing
- Is Kenscoff Manufacturing on an FDA import alert?
- No listing for Kenscoff Manufacturing 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 Kenscoff Manufacturing?
- Yes. FDA refused 1 shipment line from Kenscoff Manufacturing on January 16, 2024. The most recent, on January 16, 2024, was african spinach, dried or paste, charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Kenscoff Manufacturing's shipments?
- The most frequent charges are LIST INGRE (ingredients not listed, 1 line) and NUTRIT LBL (nutrition information missing from label, 1 line).
- What is Kenscoff Manufacturing's FEI number?
- Kenscoff Manufacturing's FDA Establishment Identifier (FEI) is 3010818478.
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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.