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Procter&Gamble Mfg Company

⚠️ Moderate Risk

FEI: 1111559 • Baltimore, MD • UNITED STATES

FEI

FEI Number

1111559

📍

Location

Baltimore, MD

🇺🇸
🏢

Address

1422 Nicholson St, , Baltimore, MD, United States

Moderate Risk

FDA Import Risk Assessment

40.5
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
5/29/2025
Latest Refusal
5/29/2025
Earliest Refusal

Score Breakdown

Violation Severity
46.7×40%
Refusal Volume
11.2×30%
Recency
87.4×20%
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).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
5/29/2025
62WBY03ALUMINUM ACETATE (SOL) (ASTRINGENT/ANTI-PERSPIRANT)
118NOT LISTED
3280FRNMFGREG
473LABELING
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

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

Procter&Gamble Mfg Company (FEI: 1111559) has 1 FDA import refusal record(s) in our database, spanning from 5/29/2025 to 5/29/2025.

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 Mfg Company's FEI number is 1111559.

What types of violations has Procter&Gamble Mfg Company received?

Procter&Gamble Mfg Company has been cited for 3 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 Mfg Company come from?

All FDA import refusal data for Procter&Gamble Mfg Company 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.