Procordia Food Ab
⚠️ Moderate Risk
FEI: 1000343819 • Eslov, Gothenberg • SWEDEN
FEI Number
1000343819
Location
Eslov, Gothenberg
Country
SWEDENAddress
Box 16, , Eslov, Gothenberg, Sweden
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
LIST INGRE
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)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
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.
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/17/2009 | 24TCE08CABBAGE (LEAF & STEM VEGETABLE) | 83NO PROCESS | Chicago District Office (CHI-DO) |
| 7/24/2008 | 24TCI08CABBAGE (LEAF & STEM VEGETABLE) | 83NO PROCESS | Chicago District Office (CHI-DO) |
| 2/25/2008 | 37JHE99SAUCES, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 2/25/2008 | 38AET99SOUP, N.E.C. | 218LIST INGRE | Los Angeles District Office (LOS-DO) |
| 2/25/2008 | 38AET99SOUP, N.E.C. | 218LIST INGRE | Los Angeles District Office (LOS-DO) |
| 8/26/2004 | 25JCE08RED BEET (ROOT & TUBER VEGETABLE) | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Procordia Food Ab's FDA import refusal history?
Procordia Food Ab (FEI: 1000343819) has 6 FDA import refusal record(s) in our database, spanning from 8/26/2004 to 2/17/2009.
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. Procordia Food Ab's FEI number is 1000343819.
What types of violations has Procordia Food Ab received?
Procordia Food Ab has been cited for 4 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 Procordia Food Ab come from?
All FDA import refusal data for Procordia Food Ab 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.