GREENYEARD PREPARED NETHERLANDSBV
⚠️ Moderate Risk
FEI: 3002808932 • Horst, Limburg • NETHERLANDS
FEI Number
3002808932
Location
Horst, Limburg
Country
NETHERLANDSAddress
Handelstraat 8, , Horst, Limburg, Netherlands
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
UNDER PRC
The article appears to have inadequate processing in having been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.
NOCONTCODE
The low acid or acidified food appears to have been prepared, packed, or held under insanitary conditions, or it may be injurious to health, due to failure to mark with a permanent container code pursuant to 21 CFR 113.60(c) or 114.80(b).
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
MFR INJ
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (the Act) in that such article appears to have been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/12/2015 | 25QEI01MUSHROOM, COMMON (AGARICUS BISPORUS), PIECES AND STEMS, SLICED | 181UNDER PRC | Cincinnati District Office (CIN-DO) |
| 2/2/2015 | 25QEE99MUSHROOMS AND OTHER FUNGI PRODUCTS, PIECES AND STEMS, SLICED, N.E.C. | 3821MFR INJ | Cincinnati District Office (CIN-DO) |
| 12/2/2014 | 25QEE99MUSHROOMS AND OTHER FUNGI PRODUCTS, PIECES AND STEMS, SLICED, N.E.C. | 160LEAK/SWELL | Cincinnati District Office (CIN-DO) |
| 12/2/2014 | 25QCE99MUSHROOMS AND OTHER FUNGI PRODUCTS, PIECES AND STEMS, SLICED, N.E.C. | 160LEAK/SWELL | Cincinnati District Office (CIN-DO) |
| 10/9/2014 | 25QEE99MUSHROOMS AND OTHER FUNGI PRODUCTS, PIECES AND STEMS, SLICED, N.E.C. | 249FILTHY | Minneapolis District Office (MIN-DO) |
| 7/24/2014 | 25PCY01MUSHROOM, COMMON (AGARICUS BISPORUS), WHOLE (BUTTON) (FUNGI) | 181UNDER PRC | Los Angeles District Office (LOS-DO) |
| 3/5/2014 | 25PCE01MUSHROOM, COMMON (AGARICUS BISPORUS), WHOLE (BUTTON) (FUNGI) | 3240NOCONTCODE | Minneapolis District Office (MIN-DO) |
| 8/6/2007 | 25QEE01MUSHROOM, COMMON (AGARICUS BISPORUS), PIECES AND STEMS, SLICED | New York District Office (NYK-DO) | |
| 8/6/2007 | 25QEE01MUSHROOM, COMMON (AGARICUS BISPORUS), PIECES AND STEMS, SLICED | New York District Office (NYK-DO) | |
| 8/20/2003 | 25QCP01MUSHROOM, COMMON (AGARICUS BISPORUS), PIECES AND STEMS, SLICED | 83NO PROCESS | New York District Office (NYK-DO) |
| 8/5/2003 | 25QCP01MUSHROOM, COMMON (AGARICUS BISPORUS), PIECES AND STEMS, SLICED | New York District Office (NYK-DO) | |
| 8/5/2003 | 25QCP01MUSHROOM, COMMON (AGARICUS BISPORUS), PIECES AND STEMS, SLICED | New York District Office (NYK-DO) | |
| 8/5/2003 | 25QCP01MUSHROOM, COMMON (AGARICUS BISPORUS), PIECES AND STEMS, SLICED | New York District Office (NYK-DO) |
Frequently Asked Questions
What is GREENYEARD PREPARED NETHERLANDSBV's FDA import refusal history?
GREENYEARD PREPARED NETHERLANDSBV (FEI: 3002808932) has 13 FDA import refusal record(s) in our database, spanning from 8/5/2003 to 3/12/2015.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. GREENYEARD PREPARED NETHERLANDSBV's FEI number is 3002808932.
What types of violations has GREENYEARD PREPARED NETHERLANDSBV received?
GREENYEARD PREPARED NETHERLANDSBV has been cited for 7 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about GREENYEARD PREPARED NETHERLANDSBV come from?
All FDA import refusal data for GREENYEARD PREPARED NETHERLANDSBV is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.