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Promoitalia Group Spa

⚠️ High Risk

FEI: 3017963076 • Milan, Milan • ITALY

FEI

FEI Number

3017963076

📍

Location

Milan, Milan

🇮🇹

Country

ITALY
🏢

Address

Via San Gregorio 44, , Milan, Milan, Italy

High Risk

FDA Import Risk Assessment

54.4
LowModerateHighCritical

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

Statistics

10
Total Refusals
5
Unique Violations
1/30/2025
Latest Refusal
7/14/2022
Earliest Refusal

Score Breakdown

Violation Severity
63.8×40%
Refusal Volume
38.6×30%
Recency
66.9×20%
Frequency
39.2×10%
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

1189×

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).

2379×

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).

32809×

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.

5084×

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.

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).

Refusal History

DateProductViolationsDivision
1/30/2025
53GY99OTHER MAKEUP PREPARATION, NOT FOR THE EYES, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/27/2024
53YY99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C.
118NOT LISTED
237NO PMA
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/27/2024
53YY99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C.
118NOT LISTED
237NO PMA
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/20/2024
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
8/7/2024
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
237NO PMA
3280FRNMFGREG
508NO 510(K)
Division of Northeast Imports (DNEI)
8/7/2024
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
237NO PMA
3280FRNMFGREG
508NO 510(K)
Division of Northeast Imports (DNEI)
8/7/2024
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
237NO PMA
3280FRNMFGREG
508NO 510(K)
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)
1/9/2024
53LC06MOISTURIZING (SKIN CARE PREPARATIONS)
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
7/14/2022
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Promoitalia Group Spa's FDA import refusal history?

Promoitalia Group Spa (FEI: 3017963076) has 10 FDA import refusal record(s) in our database, spanning from 7/14/2022 to 1/30/2025.

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. Promoitalia Group Spa's FEI number is 3017963076.

What types of violations has Promoitalia Group Spa received?

Promoitalia Group Spa 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 Promoitalia Group Spa come from?

All FDA import refusal data for Promoitalia Group Spa 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.