Protech Enterprises
✅ Low Risk
FEI: 3009020736 • Asangaon, Maharashtra • INDIA
FEI Number
3009020736
Location
Asangaon, Maharashtra
Country
INDIAAddress
9 Shiv Shakti Laghu, , Asangaon, Maharashtra, India
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
COSMETLBLG
It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/18/2014 | 53IH01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS) | Southwest Import District Office (SWI-DO) | |
| 9/6/2011 | 53IH01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS) | 475COSMETLBLG | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Protech Enterprises's FDA import refusal history?
Protech Enterprises (FEI: 3009020736) has 2 FDA import refusal record(s) in our database, spanning from 9/6/2011 to 12/18/2014.
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. Protech Enterprises's FEI number is 3009020736.
What types of violations has Protech Enterprises received?
Protech Enterprises 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 Protech Enterprises come from?
All FDA import refusal data for Protech Enterprises 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.