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Procter & Gamble

✅ Low Risk

FEI: 3005327479 • Weybridge, Surrey • UNITED KINGDOM

FEI

FEI Number

3005327479

📍

Location

Weybridge, Surrey

🇬🇧
🏢

Address

Heights Brooklands Kt13 Oxp, , Weybridge, Surrey, United Kingdom

Low Risk

FDA Import Risk Assessment

20.6
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

2
Total Refusals
2
Unique Violations
7/13/2012
Latest Refusal
1/12/2011
Earliest Refusal

Score Breakdown

Violation Severity
35.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
13.3×10%
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

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

4711×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

Refusal History

DateProductViolationsDivision
7/13/2012
53FC01HAIR DYES AND COLORS (ALL TYPES REQUIRE CAUTION STATEMENTS AND PATCH TESTS) (HAIR COLORING PREPARATI
471CSTIC LBLG
New Orleans District Office (NOL-DO)
1/12/2011
76JETPICK, MASSAGING
341REGISTERED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Procter & Gamble's FDA import refusal history?

Procter & Gamble (FEI: 3005327479) has 2 FDA import refusal record(s) in our database, spanning from 1/12/2011 to 7/13/2012.

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. Procter & Gamble's FEI number is 3005327479.

What types of violations has Procter & Gamble received?

Procter & Gamble 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 Procter & Gamble come from?

All FDA import refusal data for Procter & Gamble 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.