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Agupunt S.L.

⚠️ Moderate Risk

FEI: 3011541120 • Barcelona, Barcelona • SPAIN

FEI

FEI Number

3011541120

📍

Location

Barcelona, Barcelona

🇪🇸

Country

SPAIN
🏢

Address

Calle Casp 158, , Barcelona, Barcelona, Spain

Moderate Risk

FDA Import Risk Assessment

43.1
LowModerateHighCritical

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

Statistics

14
Total Refusals
2
Unique Violations
8/27/2020
Latest Refusal
8/27/2020
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
43.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

11814×

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).

328014×

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.

Refusal History

DateProductViolationsDivision
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/27/2020
80MQXNEEDLE, ACUPUNCTURE, SINGLE USE
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Agupunt S.L.'s FDA import refusal history?

Agupunt S.L. (FEI: 3011541120) has 14 FDA import refusal record(s) in our database, spanning from 8/27/2020 to 8/27/2020.

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. Agupunt S.L.'s FEI number is 3011541120.

What types of violations has Agupunt S.L. received?

Agupunt S.L. 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 Agupunt S.L. come from?

All FDA import refusal data for Agupunt 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.