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Industrias Coquet, S.A.

⚠️ Moderate Risk

FEI: 3003696026 • Tudela, Navarra • SPAIN

FEI

FEI Number

3003696026

📍

Location

Tudela, Navarra

🇪🇸

Country

SPAIN
🏢

Address

Plaza Sancho El Fuente 7, , Tudela, Navarra, Spain

Moderate Risk

FDA Import Risk Assessment

38.9
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

6
Total Refusals
4
Unique Violations
10/28/2013
Latest Refusal
2/19/2004
Earliest Refusal

Score Breakdown

Violation Severity
72.1×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
6.2×10%
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

836×

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.

625×

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).

2182×

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.

2601×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

Refusal History

DateProductViolationsDivision
10/28/2013
21GCT12STUFFED OLIVE (PIT FRUIT)
62NEEDS FCE
83NO PROCESS
Seattle District Office (SEA-DO)
9/26/2013
21GCT11OLIVES, GREEN, (PIT FRUIT)
218LIST INGRE
62NEEDS FCE
83NO PROCESS
Seattle District Office (SEA-DO)
7/12/2013
21GCT12STUFFED OLIVE (PIT FRUIT)
218LIST INGRE
260FALSE
62NEEDS FCE
83NO PROCESS
Seattle District Office (SEA-DO)
12/8/2011
21GCT12STUFFED OLIVE (PIT FRUIT)
62NEEDS FCE
83NO PROCESS
Seattle District Office (SEA-DO)
9/6/2011
28ACT07CAPERS, WHOLE (SPICE)
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
2/19/2004
24TAC01ARTICHOKE (LEAF & STEM VEGETABLE)
83NO PROCESS
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Industrias Coquet, S.A.'s FDA import refusal history?

Industrias Coquet, S.A. (FEI: 3003696026) has 6 FDA import refusal record(s) in our database, spanning from 2/19/2004 to 10/28/2013.

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. Industrias Coquet, S.A.'s FEI number is 3003696026.

What types of violations has Industrias Coquet, S.A. received?

Industrias Coquet, S.A. 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 Industrias Coquet, S.A. come from?

All FDA import refusal data for Industrias Coquet, 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.