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Menarini Laboratory S A

⚠️ Moderate Risk

FEI: 3005583681 • Barcelona, Barcelona • SPAIN

FEI

FEI Number

3005583681

📍

Location

Barcelona, Barcelona

🇪🇸

Country

SPAIN
🏢

Address

Calle d'Alfons XII 587, , Barcelona, Barcelona, Spain

Moderate Risk

FDA Import Risk Assessment

35.3
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
8/12/2021
Latest Refusal
1/14/2016
Earliest Refusal

Score Breakdown

Violation Severity
67.1×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
7.2×10%
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

753×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

4721×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

Refusal History

DateProductViolationsDivision
8/12/2021
65PCE03TAMSULOSIN HCL (REGULATOR)
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/10/2021
65BCL01ACETYLCYSTEINE (MUCOLYTIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/23/2017
62GCA99ANTI-INFLAMMATORY N.E.C.
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
472NO ENGLISH
Division of Northeast Imports (DNEI)
1/14/2016
62GDK99ANTI-INFLAMMATORY N.E.C.
75UNAPPROVED
Philadelphia District Office (PHI-DO)

Frequently Asked Questions

What is Menarini Laboratory S A's FDA import refusal history?

Menarini Laboratory S A (FEI: 3005583681) has 4 FDA import refusal record(s) in our database, spanning from 1/14/2016 to 8/12/2021.

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. Menarini Laboratory S A's FEI number is 3005583681.

What types of violations has Menarini Laboratory S A received?

Menarini Laboratory S A 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 Menarini Laboratory S A come from?

All FDA import refusal data for Menarini Laboratory 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.