Caviar Petrossian S. A.
⚠️ Moderate Risk
FEI: 3004306984 • Paris, Paris • FRANCE
FEI Number
3004306984
Location
Paris, Paris
Country
FRANCEAddress
Porte 47 Cap18 Voie A, 43 Rue De L Evangile, Paris, Paris, France
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
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.
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).
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 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.
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.
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.
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.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/22/2016 | 34GET99CHOCOLATE AND CHOCOLATE COVERED CANDY, WITH NUTS AND FRUIT, N.E.C. | Division of Northeast Imports (DNEI) | |
| 3/23/2012 | 36CCT04HONEY | 320LACKS FIRM | New York District Office (NYK-DO) |
| 3/23/2012 | 36CCT04HONEY | 320LACKS FIRM | New York District Office (NYK-DO) |
| 1/18/2012 | 16ACE74MONKFISH | New York District Office (NYK-DO) | |
| 1/18/2012 | 24FCE20CUCUMBERS (FRUIT USED AS VEGETABLE) | New York District Office (NYK-DO) | |
| 1/18/2012 | 24HCY01EGG PLANT, DRIED OR PASTE | 482NUTRIT LBL | New York District Office (NYK-DO) |
| 1/18/2012 | 25JCE25ONION BULB (YELLOW, WHITE, RED, ETC.) (ROOT & TUBER VEGETABLE) | New York District Office (NYK-DO) | |
| 1/18/2012 | 38AEE99SOUP, N.E.C. | New York District Office (NYK-DO) | |
| 1/18/2012 | 25SCT02TRUFFLE, FUNGI PRODUCTS, N.E.C. | New York District Office (NYK-DO) | |
| 1/18/2012 | 24TCT25SPINACH (LEAF & STEM VEGETABLE) | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Caviar Petrossian S. A.'s FDA import refusal history?
Caviar Petrossian S. A. (FEI: 3004306984) has 10 FDA import refusal record(s) in our database, spanning from 1/18/2012 to 12/22/2016.
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. Caviar Petrossian S. A.'s FEI number is 3004306984.
What types of violations has Caviar Petrossian S. A. received?
Caviar Petrossian S. A. has been cited for 8 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 Caviar Petrossian S. A. come from?
All FDA import refusal data for Caviar Petrossian S. A. 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.