Akriti Oculoplasty Logistics
⚠️ Moderate Risk
FEI: 3009621073 • Hyderabad, Telangana • INDIA
FEI Number
3009621073
Location
Hyderabad, Telangana
Country
INDIAAddress
8 - 1 - 284/Ou/232 Ou Colonyshaikpet, , Hyderabad, Telangana, 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
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).
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.
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/31/2017 | 86HLFDEVICE, MEASURING, LENS RADIUS, OPHTHALMIC | New Orleans District Office (NOL-DO) | |
| 1/31/2017 | 86HNFSCISSORS, OPHTHALMIC | New Orleans District Office (NOL-DO) | |
| 1/31/2017 | 86HNMNEEDLE, OPHTHALMIC SUTURING | New Orleans District Office (NOL-DO) | |
| 1/31/2017 | 86HLFDEVICE, MEASURING, LENS RADIUS, OPHTHALMIC | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Akriti Oculoplasty Logistics's FDA import refusal history?
Akriti Oculoplasty Logistics (FEI: 3009621073) has 4 FDA import refusal record(s) in our database, spanning from 1/31/2017 to 1/31/2017.
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. Akriti Oculoplasty Logistics's FEI number is 3009621073.
What types of violations has Akriti Oculoplasty Logistics received?
Akriti Oculoplasty Logistics has been cited for 3 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 Akriti Oculoplasty Logistics come from?
All FDA import refusal data for Akriti Oculoplasty Logistics 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.