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Pioneer Solutions

⚠️ Moderate Risk

FEI: 3011162541 • Johdpur • INDIA

FEI

FEI Number

3011162541

📍

Location

Johdpur

🇮🇳

Country

INDIA
🏢

Address

19-2 Chopsani Housing Board, , Johdpur, , India

Moderate Risk

FDA Import Risk Assessment

29.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
12/19/2014
Latest Refusal
12/19/2014
Earliest Refusal

Score Breakdown

Violation Severity
62.5×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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).

1261×

FAILS STD

The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
12/19/2014
90ITXTRANSDUCER, ULTRASONIC, DIAGNOSTIC
118NOT LISTED
126FAILS STD
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Pioneer Solutions's FDA import refusal history?

Pioneer Solutions (FEI: 3011162541) has 1 FDA import refusal record(s) in our database, spanning from 12/19/2014 to 12/19/2014.

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. Pioneer Solutions's FEI number is 3011162541.

What types of violations has Pioneer Solutions received?

Pioneer Solutions has been cited for 4 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 Pioneer Solutions come from?

All FDA import refusal data for Pioneer Solutions 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.