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INAAYA CORP

⚠️ Moderate Risk

FEI: 3009735019 • Rajkot, Gujarat • INDIA

FEI

FEI Number

3009735019

📍

Location

Rajkot, Gujarat

🇮🇳

Country

INDIA
🏢

Address

Survey, 158, No. 2, Village Taraghadi, Taluka Paddhari, Rajkot, Gujarat, India

Moderate Risk

FDA Import Risk Assessment

49.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
5/5/2016
Latest Refusal
5/5/2016
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

93×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
5/5/2016
07YET99SNACK FOODS NOT ELSEWHERE MENTIONED, N.E.C.
9SALMONELLA
Los Angeles District Office (LOS-DO)
5/5/2016
07YET99SNACK FOODS NOT ELSEWHERE MENTIONED, N.E.C.
9SALMONELLA
Los Angeles District Office (LOS-DO)
5/5/2016
07YFT99SNACK FOODS NOT ELSEWHERE MENTIONED, N.E.C.
9SALMONELLA
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is INAAYA CORP's FDA import refusal history?

INAAYA CORP (FEI: 3009735019) has 3 FDA import refusal record(s) in our database, spanning from 5/5/2016 to 5/5/2016.

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. INAAYA CORP's FEI number is 3009735019.

What types of violations has INAAYA CORP received?

INAAYA CORP 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 INAAYA CORP come from?

All FDA import refusal data for INAAYA CORP 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.