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Proctor & Gamble Home Products

⚠️ Moderate Risk

FEI: 3006262601 • Solan • INDIA

FEI

FEI Number

3006262601

📍

Location

Solan

🇮🇳

Country

INDIA
🏢

Address

Plot # 1 Industrial Area Katha Baddi, , Solan, , India

Moderate Risk

FDA Import Risk Assessment

31.3
LowModerateHighCritical

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

Statistics

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

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

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).

162×

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.

Refusal History

DateProductViolationsDivision
12/13/2011
60LBJ99ANALGESIC, N.E.C.
118NOT LISTED
16DIRECTIONS
New York District Office (NYK-DO)
12/13/2011
60LBJ99ANALGESIC, N.E.C.
118NOT LISTED
16DIRECTIONS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Proctor & Gamble Home Products's FDA import refusal history?

Proctor & Gamble Home Products (FEI: 3006262601) has 2 FDA import refusal record(s) in our database, spanning from 12/13/2011 to 12/13/2011.

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. Proctor & Gamble Home Products's FEI number is 3006262601.

What types of violations has Proctor & Gamble Home Products received?

Proctor & Gamble Home Products 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 Proctor & Gamble Home Products come from?

All FDA import refusal data for Proctor & Gamble Home Products 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.