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P.L. Centrovia

⚠️ Moderate Risk

FEI: 3009307618 • La Muela, Zaragoza • SPAIN

FEI

FEI Number

3009307618

📍

Location

La Muela, Zaragoza

🇪🇸

Country

SPAIN
🏢

Address

C/ Los Angeles 72-74, , La Muela, Zaragoza, Spain

Moderate Risk

FDA Import Risk Assessment

33.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
2/22/2012
Latest Refusal
2/22/2012
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

2382×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

4822×

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.

Refusal History

DateProductViolationsDivision
2/22/2012
12CGP15CHEESE, GOAT, N.E.C.
238UNSAFE ADD
482NUTRIT LBL
New York District Office (NYK-DO)
2/22/2012
12CGP16CHEESE, SHEEP, N.E.C.
238UNSAFE ADD
482NUTRIT LBL
New York District Office (NYK-DO)

Frequently Asked Questions

What is P.L. Centrovia's FDA import refusal history?

P.L. Centrovia (FEI: 3009307618) has 2 FDA import refusal record(s) in our database, spanning from 2/22/2012 to 2/22/2012.

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. P.L. Centrovia's FEI number is 3009307618.

What types of violations has P.L. Centrovia received?

P.L. Centrovia has been cited for 2 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 P.L. Centrovia come from?

All FDA import refusal data for P.L. Centrovia 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.