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Davis & Dann, PVT LTD.

⚠️ Moderate Risk

FEI: 3004679655 • Ruislip, Middlesex • UNITED KINGDOM

FEI

FEI Number

3004679655

📍

Location

Ruislip, Middlesex

🇬🇧
🏢

Address

Kanta House, South Ruislip; Victoria Road, Ruislip, Middlesex, United Kingdom

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

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

Score Breakdown

Violation Severity
65.0×40%
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).

3301×

UNSAFE COL

The article appears to be a color additive for the purposes of coloring only in or on drugs or devices, and is unsafe within the meaning of Section 721(a).

Refusal History

DateProductViolationsDivision
10/5/2001
62UBY99ANTI-TUSSIVE/COLD N.E.C.
118NOT LISTED
330UNSAFE COL
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Davis & Dann, PVT LTD.'s FDA import refusal history?

Davis & Dann, PVT LTD. (FEI: 3004679655) has 1 FDA import refusal record(s) in our database, spanning from 10/5/2001 to 10/5/2001.

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. Davis & Dann, PVT LTD.'s FEI number is 3004679655.

What types of violations has Davis & Dann, PVT LTD. received?

Davis & Dann, PVT 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 Davis & Dann, PVT LTD. come from?

All FDA import refusal data for Davis & Dann, PVT 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.