Pebeyre SA
⚠️ Moderate Risk
FEI: 3003574001 • Cahors, LOT • FRANCE
FEI Number
3003574001
Location
Cahors, LOT
Country
FRANCEAddress
66 Rue Frederic Suisse, , Cahors, LOT, 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
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.
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.
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.
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 |
|---|---|---|---|
| 6/18/2012 | 25PCE02TRUFFLE, WHOLE (BUTTON) (FUNGI) | 83NO PROCESS | New Orleans District Office (NOL-DO) |
| 6/18/2012 | 25SYT02TRUFFLE, FUNGI PRODUCTS, N.E.C. | New Orleans District Office (NOL-DO) | |
| 12/19/2008 | 25SET02TRUFFLE, FUNGI PRODUCTS, N.E.C. | 328USUAL NAME | New Orleans District Office (NOL-DO) |
| 6/5/2006 | 25SET02TRUFFLE, FUNGI PRODUCTS, N.E.C. | New Orleans District Office (NOL-DO) | |
| 7/3/2002 | 25PEE99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C. | 62NEEDS FCE | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Pebeyre SA's FDA import refusal history?
Pebeyre SA (FEI: 3003574001) has 5 FDA import refusal record(s) in our database, spanning from 7/3/2002 to 6/18/2012.
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. Pebeyre SA's FEI number is 3003574001.
What types of violations has Pebeyre SA received?
Pebeyre SA has been cited for 5 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 Pebeyre SA come from?
All FDA import refusal data for Pebeyre SA 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.