N.V.OVERSEAS
⚠️ Moderate Risk
FEI: 3004811787 • Delhi, Delhi • INDIA
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
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).
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.
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.
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.
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
TRANSFAT
The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/13/2007 | 63HBL08CASTOR OIL (CATHARTIC) | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 9/13/2007 | 68CAO20ANTISEPTIC USED MORE THAN 1 SPECIES | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 6/11/2007 | 21SCP05MANGO (SUBTROPICAL AND TROPICAL FRUIT) | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 6/11/2007 | 24KCE20CUCUMBERS, WITH SAUCE | Los Angeles District Office (LOS-DO) | |
| 6/11/2007 | 21SCP05MANGO (SUBTROPICAL AND TROPICAL FRUIT) | Los Angeles District Office (LOS-DO) | |
| 5/4/2007 | 24KCE20CUCUMBERS, WITH SAUCE | Los Angeles District Office (LOS-DO) | |
| 4/11/2007 | 20GCP04LEMON (CITRUS) | Los Angeles District Office (LOS-DO) | |
| 4/11/2007 | 24KCE20CUCUMBERS, WITH SAUCE | Los Angeles District Office (LOS-DO) | |
| 4/11/2007 | 24KCE20CUCUMBERS, WITH SAUCE | Los Angeles District Office (LOS-DO) | |
| 4/11/2007 | 21SCP05MANGO (SUBTROPICAL AND TROPICAL FRUIT) | Los Angeles District Office (LOS-DO) | |
| 4/11/2007 | 24KCE08PEPPER, HOT, WITH SAUCE | Los Angeles District Office (LOS-DO) | |
| 4/11/2007 | 24KCE08PEPPER, HOT, WITH SAUCE | Los Angeles District Office (LOS-DO) | |
| 4/11/2007 | 25HCE99MIXED VEGETABLES, WITH SAUCE, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 4/11/2007 | 21SCP05MANGO (SUBTROPICAL AND TROPICAL FRUIT) | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is N.V.OVERSEAS's FDA import refusal history?
N.V.OVERSEAS (FEI: 3004811787) has 14 FDA import refusal record(s) in our database, spanning from 4/11/2007 to 9/13/2007.
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. N.V.OVERSEAS's FEI number is 3004811787.
What types of violations has N.V.OVERSEAS received?
N.V.OVERSEAS 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 N.V.OVERSEAS come from?
All FDA import refusal data for N.V.OVERSEAS 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.