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REVIVE INNOVATIONS PVT LTD

⚠️ High Risk

FEI: 3030805389 • Rajkot, Gujarat • INDIA

FEI

FEI Number

3030805389

📍

Location

Rajkot, Gujarat

🇮🇳

Country

INDIA
🏢

Address

5 1 1 Gomta Charkhadi Gondal Virpur Natio, Nehru Nagar Plot No -2; Survey No 121, Rajkot, Gujarat, India

High Risk

FDA Import Risk Assessment

55.5
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
10/27/2025
Latest Refusal
10/27/2025
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
11.2×30%
Recency
95.7×20%
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

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
10/27/2025
29AGT99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is REVIVE INNOVATIONS PVT LTD's FDA import refusal history?

REVIVE INNOVATIONS PVT LTD (FEI: 3030805389) has 1 FDA import refusal record(s) in our database, spanning from 10/27/2025 to 10/27/2025.

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. REVIVE INNOVATIONS PVT LTD's FEI number is 3030805389.

What types of violations has REVIVE INNOVATIONS PVT LTD received?

REVIVE INNOVATIONS PVT LTD 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 REVIVE INNOVATIONS PVT LTD come from?

All FDA import refusal data for REVIVE INNOVATIONS PVT 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.