PROCTOR AND GAMBLE MANUFACTURING
⚠️ High Risk
FEI: 3038156774 • Ahmedabad • INDIA
FEI Number
3038156774
Location
Ahmedabad
Country
INDIAAddress
Gillette Diversified Op, , Ahmedabad, , India
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
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
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).
Refusal History
Frequently Asked Questions
What is PROCTOR AND GAMBLE MANUFACTURING's FDA import refusal history?
PROCTOR AND GAMBLE MANUFACTURING (FEI: 3038156774) has 2 FDA import refusal record(s) in our database, spanning from 6/4/2025 to 6/4/2025.
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. PROCTOR AND GAMBLE MANUFACTURING's FEI number is 3038156774.
What types of violations has PROCTOR AND GAMBLE MANUFACTURING received?
PROCTOR AND GAMBLE MANUFACTURING 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 AND GAMBLE MANUFACTURING come from?
All FDA import refusal data for PROCTOR AND GAMBLE MANUFACTURING 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.