ImportRefusal LogoImportRefusal

PRIMUS REMEDIES

⚠️ High Risk

FEI: 3016938925 • Hyderabad, Telangana • INDIA

FEI

FEI Number

3016938925

📍

Location

Hyderabad, Telangana

🇮🇳

Country

INDIA
🏢

Address

A 2nd, 1 16 H No 2 - 3 - 64, Hyderabad, Telangana, India

High Risk

FDA Import Risk Assessment

50.8
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
8/26/2025
Latest Refusal
8/26/2025
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
92.3×20%
Frequency
10.0×10%
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

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).

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
8/26/2025
61PDB99ANTI-DIABETIC N.E.C.
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is PRIMUS REMEDIES's FDA import refusal history?

PRIMUS REMEDIES (FEI: 3016938925) has 1 FDA import refusal record(s) in our database, spanning from 8/26/2025 to 8/26/2025.

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. PRIMUS REMEDIES's FEI number is 3016938925.

What types of violations has PRIMUS REMEDIES received?

PRIMUS REMEDIES has been cited for 2 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 PRIMUS REMEDIES come from?

All FDA import refusal data for PRIMUS REMEDIES 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.