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Luis Penalva, S.L.

⚠️ Moderate Risk

FEI: 3004298259 • Novelda, Alicante • SPAIN

FEI

FEI Number

3004298259

📍

Location

Novelda, Alicante

🇪🇸

Country

SPAIN
🏢

Address

Plaza De La Magdalena 13, , Novelda, Alicante, Spain

Moderate Risk

FDA Import Risk Assessment

49.3
LowModerateHighCritical

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

Statistics

7
Total Refusals
4
Unique Violations
12/12/2023
Latest Refusal
2/3/2014
Earliest Refusal

Score Breakdown

Violation Severity
67.1×40%
Refusal Volume
33.5×30%
Recency
58.3×20%
Frequency
7.1×10%
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

553×

OMITTED

The article is subject to refusal of admission pursuant Section 801(a)(3) of the FD&C Act in that it appears that a valuable constituent of the article has been in whole or in part omitted or abstracted from the article.

832×

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.

3241×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

91×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
12/12/2023
28AEH40SAFFRON, WHOLE (SPICE)
55OMITTED
Division of Southeast Imports (DSEI)
12/12/2023
28AEH40SAFFRON, WHOLE (SPICE)
55OMITTED
Division of Southeast Imports (DSEI)
12/12/2023
28AFH40SAFFRON, WHOLE (SPICE)
55OMITTED
Division of Southeast Imports (DSEI)
6/10/2016
28BEH33PAPRIKA, GROUND, CRACKED (SPICE)
9SALMONELLA
San Francisco District Office (SAN-DO)
2/2/2016
28BHT33PAPRIKA, GROUND, CRACKED (SPICE)
324NO ENGLISH
New England District Office (NWE-DO)
2/3/2014
28ACY99WHOLE SPICE, N.E.C.
83NO PROCESS
San Francisco District Office (SAN-DO)
2/3/2014
28ACY07CAPERS, WHOLE (SPICE)
83NO PROCESS
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Luis Penalva, S.L.'s FDA import refusal history?

Luis Penalva, S.L. (FEI: 3004298259) has 7 FDA import refusal record(s) in our database, spanning from 2/3/2014 to 12/12/2023.

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. Luis Penalva, S.L.'s FEI number is 3004298259.

What types of violations has Luis Penalva, S.L. received?

Luis Penalva, S.L. 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 Luis Penalva, S.L. come from?

All FDA import refusal data for Luis Penalva, S.L. 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.