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P C Products Srl

⚠️ Moderate Risk

FEI: 3006625782 • Desio, Monza E della Brianza • ITALY

FEI

FEI Number

3006625782

📍

Location

Desio, Monza E della Brianza

🇮🇹

Country

ITALY
🏢

Address

Via Molinara 1, , Desio, Monza E della Brianza, Italy

Moderate Risk

FDA Import Risk Assessment

49.4
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
10/24/2025
Latest Refusal
11/9/2020
Earliest Refusal

Score Breakdown

Violation Severity
61.3×40%
Refusal Volume
25.9×30%
Recency
81.5×20%
Frequency
8.1×10%
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

754×

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).

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).

22803×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.

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.

3362×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

Refusal History

DateProductViolationsDivision
10/24/2025
64LCJ67CLOBETASOL PROPIONATE (GLUCOCORTICOID)
75UNAPPROVED
Division of Northeast Imports (DNEI)
8/31/2021
64LCJ67CLOBETASOL PROPIONATE (GLUCOCORTICOID)
118NOT LISTED
2280DIRSEXMPT
3280FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
11/9/2020
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
118NOT LISTED
2280DIRSEXMPT
3280FRNMFGREG
336INCONSPICU
75UNAPPROVED
Division of Northeast Imports (DNEI)
11/9/2020
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
118NOT LISTED
2280DIRSEXMPT
3280FRNMFGREG
336INCONSPICU
75UNAPPROVED
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is P C Products Srl's FDA import refusal history?

P C Products Srl (FEI: 3006625782) has 4 FDA import refusal record(s) in our database, spanning from 11/9/2020 to 10/24/2025.

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. P C Products Srl's FEI number is 3006625782.

What types of violations has P C Products Srl received?

P C Products Srl 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 P C Products Srl come from?

All FDA import refusal data for P C Products Srl 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.