Ayn & Getti P. Ltd.
⚠️ Moderate Risk
FEI: 3006059282 • Bombay • INDIA
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
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.
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).
COSM COLOR
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).
COLOR LBLG
The color additive appears to not have its packaging and labeling in conformity with such requirements as issued under section 721.
POISONOUS
The article is subject to refusal of admission pursuant Section 801(a)(3) in that The cosmetic appears to bear or contain a poisonous or deleterious substance which may render it injurious to users under the conditions prescribed in the labeling thereof, or, under such conditions of use as are customary or usual.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/31/2007 | 53CD02EYELINER (EYE MAKEUP PREPARATIONS) | Seattle District Office (SEA-DO) | |
| 5/3/2007 | 53CH02EYELINER (EYE MAKEUP PREPARATIONS) | Baltimore District Office (BLT-DO) | |
| 4/5/2007 | 53CH02EYELINER (EYE MAKEUP PREPARATIONS) | 471CSTIC LBLG | Baltimore District Office (BLT-DO) |
Frequently Asked Questions
What is Ayn & Getti P. Ltd.'s FDA import refusal history?
Ayn & Getti P. Ltd. (FEI: 3006059282) has 3 FDA import refusal record(s) in our database, spanning from 4/5/2007 to 10/31/2007.
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. Ayn & Getti P. Ltd.'s FEI number is 3006059282.
What types of violations has Ayn & Getti P. Ltd. received?
Ayn & Getti P. Ltd. has been cited for 5 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 Ayn & Getti P. Ltd. come from?
All FDA import refusal data for Ayn & Getti P. Ltd. 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.