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Ultratech India Ltd.

⚠️ Moderate Risk

FEI: 3003735154 • Navi Mumbai, Maharashtra • INDIA

FEI

FEI Number

3003735154

📍

Location

Navi Mumbai, Maharashtra

🇮🇳

Country

INDIA
🏢

Address

113 J K Chambers Sector - 17, , Vashi, Navi Mumbai, Maharashtra, India

Moderate Risk

FDA Import Risk Assessment

33.9
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

3
Total Refusals
4
Unique Violations
6/27/2016
Latest Refusal
12/11/2013
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
11.8×10%
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

1181×

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).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

35001×

RXLABEL

The labeling fails to bear, at a minimum, the symbol "RX Only".

751×

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

DateProductViolationsDivision
6/27/2016
66SCT51TADALAFIL
16DIRECTIONS
New York District Office (NYK-DO)
10/28/2014
65PCS02SILDENAFIL CITRATE (REGULATOR)
118NOT LISTED
3500RXLABEL
New Orleans District Office (NOL-DO)
12/11/2013
53LC99OTHER SKIN CARE PREPARATIONS, N.E.C.
75UNAPPROVED
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Ultratech India Ltd.'s FDA import refusal history?

Ultratech India Ltd. (FEI: 3003735154) has 3 FDA import refusal record(s) in our database, spanning from 12/11/2013 to 6/27/2016.

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. Ultratech India Ltd.'s FEI number is 3003735154.

What types of violations has Ultratech India Ltd. received?

Ultratech India Ltd. has been cited for 4 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 Ultratech India Ltd. come from?

All FDA import refusal data for Ultratech India 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.