Frubaca-Cooperativa de Hortofruticultores, CRL
⚠️ Moderate Risk
FEI: 3011926708 • Alcobaca, Leiria • PORTUGAL
FEI Number
3011926708
Location
Alcobaca, Leiria
Country
PORTUGALAddress
Acipreste, , Alcobaca, Leiria, Portugal
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
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.
USUAL NAME
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
LACKS N/C
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
LACKS FIRM
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/22/2017 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | 306INSANITARY | Division of Southeast Imports (DSEI) |
| 3/22/2017 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | 306INSANITARY | Division of Southeast Imports (DSEI) |
| 3/22/2017 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | 306INSANITARY | Division of Southeast Imports (DSEI) |
| 3/22/2017 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | 306INSANITARY | Division of Southeast Imports (DSEI) |
| 3/22/2017 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | 306INSANITARY | Division of Southeast Imports (DSEI) |
| 3/22/2017 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | 306INSANITARY | Division of Southeast Imports (DSEI) |
| 11/14/2016 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | Philadelphia District Office (PHI-DO) | |
| 11/14/2016 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | Philadelphia District Office (PHI-DO) | |
| 11/14/2016 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | Philadelphia District Office (PHI-DO) | |
| 11/14/2016 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | Philadelphia District Office (PHI-DO) | |
| 11/14/2016 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | 473LABELING | Philadelphia District Office (PHI-DO) |
| 11/14/2016 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | 473LABELING | Philadelphia District Office (PHI-DO) |
| 11/14/2016 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | 473LABELING | Philadelphia District Office (PHI-DO) |
| 11/14/2016 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | 473LABELING | Philadelphia District Office (PHI-DO) |
| 11/14/2016 | 20SGT01APPLE, CORE FRUIT JUICES OR CONCENTRATES | 473LABELING | Philadelphia District Office (PHI-DO) |
| 9/16/2016 | 20SGC01APPLE, CORE FRUIT JUICES OR CONCENTRATES | Philadelphia District Office (PHI-DO) | |
| 9/16/2016 | 20SGC01APPLE, CORE FRUIT JUICES OR CONCENTRATES | Philadelphia District Office (PHI-DO) | |
| 9/16/2016 | 20SGC01APPLE, CORE FRUIT JUICES OR CONCENTRATES | Philadelphia District Office (PHI-DO) | |
| 9/16/2016 | 20SGC01APPLE, CORE FRUIT JUICES OR CONCENTRATES | Philadelphia District Office (PHI-DO) | |
| 9/16/2016 | 20SGC01APPLE, CORE FRUIT JUICES OR CONCENTRATES | Philadelphia District Office (PHI-DO) |
Frequently Asked Questions
What is Frubaca-Cooperativa de Hortofruticultores, CRL's FDA import refusal history?
Frubaca-Cooperativa de Hortofruticultores, CRL (FEI: 3011926708) has 20 FDA import refusal record(s) in our database, spanning from 9/16/2016 to 3/22/2017.
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. Frubaca-Cooperativa de Hortofruticultores, CRL's FEI number is 3011926708.
What types of violations has Frubaca-Cooperativa de Hortofruticultores, CRL received?
Frubaca-Cooperativa de Hortofruticultores, CRL 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 Frubaca-Cooperativa de Hortofruticultores, CRL come from?
All FDA import refusal data for Frubaca-Cooperativa de Hortofruticultores, CRL 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.