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Proctor & Gamble Manufactura, S. De R.L. De C.V.

✅ Low Risk

FEI: 3003678546 • Hidalgo • MEXICO

FEI

FEI Number

3003678546

📍

Location

Hidalgo

🇲🇽

Country

MEXICO
🏢

Address

Parque Industrial Tepeji, Km 60.5, Carretera Mexico-Queretaro, Calle Nortes, Municipio Tepesi Del Rio, Hidalgo, , Mexico

Low Risk

FDA Import Risk Assessment

23.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
3/21/2011
Latest Refusal
3/21/2011
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
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

4712×

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
3/21/2011
53ED99OTHER HAIR PREPARATIONS, NON-COLORING), N.E.C.
471CSTIC LBLG
Florida District Office (FLA-DO)
3/21/2011
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
471CSTIC LBLG
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Proctor & Gamble Manufactura, S. De R.L. De C.V.'s FDA import refusal history?

Proctor & Gamble Manufactura, S. De R.L. De C.V. (FEI: 3003678546) has 2 FDA import refusal record(s) in our database, spanning from 3/21/2011 to 3/21/2011.

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 Manufactura, S. De R.L. De C.V.'s FEI number is 3003678546.

What types of violations has Proctor & Gamble Manufactura, S. De R.L. De C.V. received?

Proctor & Gamble Manufactura, S. De R.L. De C.V. has been cited for 1 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 Manufactura, S. De R.L. De C.V. come from?

All FDA import refusal data for Proctor & Gamble Manufactura, S. De R.L. De C.V. 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.