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Procter & Gamble Manufacturing GmbH

⚠️ Moderate Risk

FEI: 3000302531 • Marktheidenfeld, Bavaria • GERMANY

FEI

FEI Number

3000302531

📍

Location

Marktheidenfeld, Bavaria

🇩🇪

Country

GERMANY
🏢

Address

Baumhofstr. 40, , Marktheidenfeld, Bavaria, Germany

Moderate Risk

FDA Import Risk Assessment

45.0
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
7/12/2023
Latest Refusal
6/12/2023
Earliest Refusal

Score Breakdown

Violation Severity
58.2×40%
Refusal Volume
25.9×30%
Recency
50.0×20%
Frequency
40.0×10%
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

1184×

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).

30003×

N-RX INACT

The article appears to be a nonprescription drug and fails to bear the established name of each inactive ingredient in alphabetical order on the outside container of the retail package.

753×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

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.

Refusal History

DateProductViolationsDivision
7/12/2023
76JEQTOOTHBRUSH, POWERED
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
6/12/2023
63RAY04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC)
118NOT LISTED
3000N-RX INACT
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/12/2023
63RAY04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC)
118NOT LISTED
3000N-RX INACT
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/12/2023
63RBY04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC)
118NOT LISTED
3000N-RX INACT
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

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

Procter & Gamble Manufacturing GmbH (FEI: 3000302531) has 4 FDA import refusal record(s) in our database, spanning from 6/12/2023 to 7/12/2023.

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 Manufacturing GmbH's FEI number is 3000302531.

What types of violations has Procter & Gamble Manufacturing GmbH received?

Procter & Gamble Manufacturing GmbH has been cited for 4 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 Manufacturing GmbH come from?

All FDA import refusal data for Procter & Gamble Manufacturing GmbH 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.