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PROFESSIONAL DERMA SA

⚠️ High Risk

FEI: 3014401685 • Lugand • SWITZERLAND

FEI

FEI Number

3014401685

📍

Location

Lugand

🇨🇭
🏢

Address

Riva A Caccia 1o, , Lugand, , Switzerland

High Risk

FDA Import Risk Assessment

51.9
LowModerateHighCritical

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

Statistics

5
Total Refusals
5
Unique Violations
11/19/2025
Latest Refusal
1/19/2024
Earliest Refusal

Score Breakdown

Violation Severity
52.9×40%
Refusal Volume
28.8×30%
Recency
97.1×20%
Frequency
27.2×10%
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

2374×

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).

1183×

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).

32803×

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.

32602×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

3412×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

Refusal History

DateProductViolationsDivision
11/19/2025
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
3260NO ENGLISH
Division of Southeast Imports (DSEI)
5/20/2024
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
237NO PMA
Division of Northeast Imports (DNEI)
4/11/2024
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
237NO PMA
3280FRNMFGREG
341REGISTERED
Division of Southeast Imports (DSEI)
4/5/2024
53YY99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C.
118NOT LISTED
237NO PMA
3260NO ENGLISH
3280FRNMFGREG
Division of Southeast Imports (DSEI)
1/19/2024
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
237NO PMA
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is PROFESSIONAL DERMA SA's FDA import refusal history?

PROFESSIONAL DERMA SA (FEI: 3014401685) has 5 FDA import refusal record(s) in our database, spanning from 1/19/2024 to 11/19/2025.

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. PROFESSIONAL DERMA SA's FEI number is 3014401685.

What types of violations has PROFESSIONAL DERMA SA received?

PROFESSIONAL DERMA SA 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 PROFESSIONAL DERMA SA come from?

All FDA import refusal data for PROFESSIONAL DERMA SA 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.