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Proteos Biotech SL

⚠️ High Risk

FEI: 3009228570 • Albacete, Albacete • SPAIN

FEI

FEI Number

3009228570

📍

Location

Albacete, Albacete

🇪🇸

Country

SPAIN
🏢

Address

Polig. Industrial Romica, Calle Dublin, 58, Albacete, Albacete, Spain

High Risk

FDA Import Risk Assessment

55.5
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

3
Total Refusals
5
Unique Violations
10/29/2025
Latest Refusal
7/26/2024
Earliest Refusal

Score Breakdown

Violation Severity
68.3×40%
Refusal Volume
22.3×30%
Recency
95.6×20%
Frequency
23.8×10%
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

5082×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

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).

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

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.

751×

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).

Refusal History

DateProductViolationsDivision
10/29/2025
87MOZACID, HYALURONIC, INTRAARTICULAR
508NO 510(K)
Division of Northeast Imports (DNEI)
10/29/2025
58ICP26COLLAGENASE
75UNAPPROVED
Division of Northeast Imports (DNEI)
7/26/2024
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
237NO PMA
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Proteos Biotech SL's FDA import refusal history?

Proteos Biotech SL (FEI: 3009228570) has 3 FDA import refusal record(s) in our database, spanning from 7/26/2024 to 10/29/2025.

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. Proteos Biotech SL's FEI number is 3009228570.

What types of violations has Proteos Biotech SL received?

Proteos Biotech SL 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 Proteos Biotech SL come from?

All FDA import refusal data for Proteos Biotech SL 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.