ImportRefusal LogoImportRefusal

Nivik

⚠️ Moderate Risk

FEI: 3008082963 • Shivpuri • INDIA

FEI

FEI Number

3008082963

📍

Location

Shivpuri

🇮🇳

Country

INDIA
🏢

Address

52 Raghvendra Nagar, , Shivpuri, , India

Moderate Risk

FDA Import Risk Assessment

28.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
4/9/2010
Latest Refusal
4/9/2010
Earliest Refusal

Score Breakdown

Violation Severity
47.5×40%
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

1182×

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).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
4/9/2010
65LAJ99PROTECTANT N.E.C.
118NOT LISTED
Florida District Office (FLA-DO)
4/9/2010
65LAJ99PROTECTANT N.E.C.
118NOT LISTED
Florida District Office (FLA-DO)
4/9/2010
65LAR99PROTECTANT N.E.C.
16DIRECTIONS
333LACKS FIRM
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Nivik's FDA import refusal history?

Nivik (FEI: 3008082963) has 3 FDA import refusal record(s) in our database, spanning from 4/9/2010 to 4/9/2010.

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. Nivik's FEI number is 3008082963.

What types of violations has Nivik received?

Nivik has been cited for 3 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 Nivik come from?

All FDA import refusal data for Nivik 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.