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NORTON (WATERFORD) LIMITED

⚠️ Moderate Risk

FEI: 3002807777 • Waterford, Co. WATERFORD • IRELAND

FEI

FEI Number

3002807777

📍

Location

Waterford, Co. WATERFORD

🇮🇪

Country

IRELAND
🏢

Address

Unit 301, Waterford Industrial Park; Cork Road, Waterford, Co. WATERFORD, Ireland

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

11
Total Refusals
4
Unique Violations
5/1/2018
Latest Refusal
4/12/2002
Earliest Refusal

Score Breakdown

Violation Severity
69.0×40%
Refusal Volume
40.0×30%
Recency
0.0×20%
Frequency
6.8×10%
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

1188×

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).

758×

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).

163×

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.

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
5/1/2018
63BCY01ALBUTEROL (BRONCHODILATOR)
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/26/2018
63BCQ02ALBUTEROL SULFATE (BRONCHODILATOR)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/18/2015
64LDQ02BECLOMETHASONE DIPROPIONATE (GLUCOCORTICOID)
75UNAPPROVED
Cincinnati District Office (CIN-DO)
12/10/2012
66VCA99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
Chicago District Office (CHI-DO)
12/10/2012
66VCA99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
Chicago District Office (CHI-DO)
12/10/2012
66VCA99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
Chicago District Office (CHI-DO)
9/10/2008
66VIP99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New Orleans District Office (NOL-DO)
5/30/2008
63BDZ25FLUTICASONE PROPIONATE (BRONCHODILATOR)
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
3/30/2005
63BCV01ALBUTEROL (BRONCHODILATOR)
118NOT LISTED
Florida District Office (FLA-DO)
4/12/2002
65KCA99PROSTAGLANDIN N.E.C.
118NOT LISTED
Chicago District Office (CHI-DO)
4/12/2002
65KCA99PROSTAGLANDIN N.E.C.
118NOT LISTED
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is NORTON (WATERFORD) LIMITED's FDA import refusal history?

NORTON (WATERFORD) LIMITED (FEI: 3002807777) has 11 FDA import refusal record(s) in our database, spanning from 4/12/2002 to 5/1/2018.

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. NORTON (WATERFORD) LIMITED's FEI number is 3002807777.

What types of violations has NORTON (WATERFORD) LIMITED received?

NORTON (WATERFORD) LIMITED 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 NORTON (WATERFORD) LIMITED come from?

All FDA import refusal data for NORTON (WATERFORD) LIMITED 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.