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Acme Lifetech LLP

⚠️ High Risk

FEI: 3013998702 • Baddi, Himachal Pradesh • INDIA

FEI

FEI Number

3013998702

📍

Location

Baddi, Himachal Pradesh

🇮🇳

Country

INDIA
🏢

Address

104 105 Plot No 103, , Baddi, Himachal Pradesh, India

High Risk

FDA Import Risk Assessment

58.0
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

3
Total Refusals
1
Unique Violations
7/3/2025
Latest Refusal
3/16/2017
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
74.7×20%
Frequency
3.6×10%
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

753×

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
7/3/2025
66VIY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/14/2020
61TDA31DOMPERIDONE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/16/2017
61TDY31DOMPERIDONE
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Acme Lifetech LLP's FDA import refusal history?

Acme Lifetech LLP (FEI: 3013998702) has 3 FDA import refusal record(s) in our database, spanning from 3/16/2017 to 7/3/2025.

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. Acme Lifetech LLP's FEI number is 3013998702.

What types of violations has Acme Lifetech LLP received?

Acme Lifetech LLP has been cited for 1 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 Acme Lifetech LLP come from?

All FDA import refusal data for Acme Lifetech LLP 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.