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Miraculins Inc

⚠️ Moderate Risk

FEI: 3010116263 • Winnipeg, MB • CANADA

FEI

FEI Number

3010116263

📍

Location

Winnipeg, MB

🇨🇦

Country

CANADA
🏢

Address

Unit 201 179 Mcdermot Ave, , Winnipeg, MB, Canada

Moderate Risk

FDA Import Risk Assessment

29.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
8/28/2015
Latest Refusal
8/28/2015
Earliest Refusal

Score Breakdown

Violation Severity
62.5×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

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).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

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.

Refusal History

DateProductViolationsDivision
8/28/2015
86NFGDEVICE, COMMUNICATIONS, IMAGES, OPHTHALMIC
118NOT LISTED
16DIRECTIONS
237NO PMA
3280FRNMFGREG
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Miraculins Inc's FDA import refusal history?

Miraculins Inc (FEI: 3010116263) has 1 FDA import refusal record(s) in our database, spanning from 8/28/2015 to 8/28/2015.

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. Miraculins Inc's FEI number is 3010116263.

What types of violations has Miraculins Inc received?

Miraculins Inc has been cited for 4 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 Miraculins Inc come from?

All FDA import refusal data for Miraculins Inc 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.