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Slater & Frith Ltd.

⚠️ Moderate Risk

FEI: 1000437071 • Norwich • UNITED KINGDOM

FEI

FEI Number

1000437071

📍

Location

Norwich

🇬🇧
🏢

Address

Lurista House, Stalham Road, , Norwich, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

33.5
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
1/5/2011
Latest Refusal
10/16/2001
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
2.2×10%
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).

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
1/5/2011
61TSY29SCOPOLAMINE (ANTI-EMETIC/NAUSEANT)
118NOT LISTED
New Orleans District Office (NOL-DO)
10/16/2001
66VCR99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Slater & Frith Ltd.'s FDA import refusal history?

Slater & Frith Ltd. (FEI: 1000437071) has 2 FDA import refusal record(s) in our database, spanning from 10/16/2001 to 1/5/2011.

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. Slater & Frith Ltd.'s FEI number is 1000437071.

What types of violations has Slater & Frith Ltd. received?

Slater & Frith Ltd. 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 Slater & Frith Ltd. come from?

All FDA import refusal data for Slater & Frith Ltd. 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.