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SWEETCARE LDA

⚠️ High Risk

FEI: 3019687136 • Porto • PORTUGAL

FEI

FEI Number

3019687136

📍

Location

Porto

🇵🇹

Country

PORTUGAL
🏢

Address

Rua Dr Eduardo Santos S, , Porto, , Portugal

High Risk

FDA Import Risk Assessment

55.2
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
9/24/2025
Latest Refusal
7/3/2025
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
17.7×30%
Recency
79.7×20%
Frequency
20.0×10%
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

5081×

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.

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
9/24/2025
85HISCONDOM
508NO 510(K)
Division of Southeast Imports (DSEI)
7/3/2025
63NDK04DEXPANTHENOL (CHOLINERGIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SWEETCARE LDA's FDA import refusal history?

SWEETCARE LDA (FEI: 3019687136) has 2 FDA import refusal record(s) in our database, spanning from 7/3/2025 to 9/24/2025.

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. SWEETCARE LDA's FEI number is 3019687136.

What types of violations has SWEETCARE LDA received?

SWEETCARE LDA 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 SWEETCARE LDA come from?

All FDA import refusal data for SWEETCARE LDA 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.