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Molekula

⚠️ Moderate Risk

FEI: 3011497125 • Newcastle upon Tyne • UNITED KINGDOM

FEI

FEI Number

3011497125

📍

Location

Newcastle upon Tyne

🇬🇧
🏢

Address

Unit 2, Balliol Business Park; Benton Lane, Newcastle upon Tyne, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

35.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
4/16/2018
Latest Refusal
7/21/2015
Earliest Refusal

Score Breakdown

Violation Severity
68.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
10.9×10%
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

1182×

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.

721×

NEW VET DR

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.

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
4/16/2018
60HAY99ALDOSTERONE ANTAGONIST, N.E.C.
118NOT LISTED
16DIRECTIONS
Division of Northern Border Imports (DNBI)
6/5/2017
64TOY04MYCOPHENOLATE MOFETIL (IMMUNOSUPPRESSIVE)
72NEW VET DR
Division of Southeast Imports (DSEI)
7/21/2015
60HIY99ALDOSTERONE ANTAGONIST, N.E.C.
118NOT LISTED
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Molekula's FDA import refusal history?

Molekula (FEI: 3011497125) has 3 FDA import refusal record(s) in our database, spanning from 7/21/2015 to 4/16/2018.

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. Molekula's FEI number is 3011497125.

What types of violations has Molekula received?

Molekula 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 Molekula come from?

All FDA import refusal data for Molekula 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.