Dr. Mann Pharma
⚠️ Moderate Risk
FEI: 3002790083 • Berlin • GERMANY
FEI Number
3002790083
Location
Berlin
Country
GERMANYAddress
Fabrik Gmbh, 13581, , Berlin, , Germany
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
Refusal History
Frequently Asked Questions
What is Dr. Mann Pharma's FDA import refusal history?
Dr. Mann Pharma (FEI: 3002790083) has 2 FDA import refusal record(s) in our database, spanning from 2/25/2003 to 2/25/2003.
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. Dr. Mann Pharma's FEI number is 3002790083.
What types of violations has Dr. Mann Pharma received?
Dr. Mann Pharma 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 Dr. Mann Pharma come from?
All FDA import refusal data for Dr. Mann Pharma 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.