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Relaxpharmaceuticals

⚠️ Moderate Risk

FEI: 3007532922 • Himachal • INDIA

FEI

FEI Number

3007532922

📍

Location

Himachal

🇮🇳

Country

INDIA
🏢

Address

49a-B Godpur Industrial Area, , Himachal, , India

Moderate Risk

FDA Import Risk Assessment

47.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
1/4/2011
Latest Refusal
1/4/2011
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

754×

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
1/4/2011
60LDE04ANTIPYRINE (ANALGESIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
1/4/2011
66MDE03ALPRAZOLAM (TRANQUILIZER)
75UNAPPROVED
New Orleans District Office (NOL-DO)
1/4/2011
56CDE71CEFUROXIME AXETIL (CEPHALOSPORINS)
75UNAPPROVED
New Orleans District Office (NOL-DO)
1/4/2011
56CDE71CEFUROXIME AXETIL (CEPHALOSPORINS)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Relaxpharmaceuticals's FDA import refusal history?

Relaxpharmaceuticals (FEI: 3007532922) has 4 FDA import refusal record(s) in our database, spanning from 1/4/2011 to 1/4/2011.

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. Relaxpharmaceuticals's FEI number is 3007532922.

What types of violations has Relaxpharmaceuticals received?

Relaxpharmaceuticals 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 Relaxpharmaceuticals come from?

All FDA import refusal data for Relaxpharmaceuticals 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.