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SAANVI INC

Low Risk

FEI: 3017174047 • New Delhi • INDIA

FEI

FEI Number

3017174047

📍

Location

New Delhi

🇮🇳

Country

INDIA
🏢

Address

Center Point Saanvi A 8, Opposite Udyog Nagar Metro Stati, New Delhi, , India

Low Risk

FDA Import Risk Assessment

21.9
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
5
Unique Violations
10/2/2020
Latest Refusal
10/2/2020
Earliest Refusal

Score Breakdown

Violation Severity
44.0×40%
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).

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.

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.

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

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
10/2/2020
80FXXMASK, SURGICAL
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
341REGISTERED
508NO 510(K)
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is SAANVI INC's FDA import refusal history?

SAANVI INC (FEI: 3017174047) has 1 FDA import refusal record(s) in our database, spanning from 10/2/2020 to 10/2/2020.

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. SAANVI INC's FEI number is 3017174047.

What types of violations has SAANVI INC received?

SAANVI INC has been cited for 5 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 SAANVI INC come from?

All FDA import refusal data for SAANVI INC 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.