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JAIRAMDASS KHUSHIRAM

⚠️ Moderate Risk

FEI: 3012742822 • Navi Mumbai, Maharashtra • INDIA

FEI

FEI Number

3012742822

📍

Location

Navi Mumbai, Maharashtra

🇮🇳

Country

INDIA
🏢

Address

5 Shri Mokam Bika Mandir Marg, , Navi Mumbai, Maharashtra, India

Moderate Risk

FDA Import Risk Assessment

44.5
LowModerateHighCritical

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

Statistics

10
Total Refusals
3
Unique Violations
12/29/2017
Latest Refusal
12/29/2017
Earliest Refusal

Score Breakdown

Violation Severity
57.2×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

386410×

NCONTACT

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.

38638×

PLANT PART

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(C) of the FD&C Act in that the supplement contains an herb or other botanical described in section 201(ff)(1)(C), and the label or labeling of the supplement fails to identify any part of the plant from which the ingredient is derived.

757×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
12/29/2017
54KCH04FANG FENG (HERBAL & BOTANICALS, NOT TEAS II)
3864NCONTACT
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/29/2017
54FCH99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
3864NCONTACT
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/29/2017
54FCH99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
3863PLANT PART
3864NCONTACT
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/29/2017
54FCH99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
3863PLANT PART
3864NCONTACT
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/29/2017
54FCP99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
3863PLANT PART
3864NCONTACT
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/29/2017
54FCH99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
3863PLANT PART
3864NCONTACT
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/29/2017
54FCY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
3863PLANT PART
3864NCONTACT
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/29/2017
54FCH99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
3863PLANT PART
3864NCONTACT
Division of Southeast Imports (DSEI)
12/29/2017
54FCH89TRIBULUS (HERBAL & BOTANICALS, NOT TEAS)
3863PLANT PART
3864NCONTACT
Division of Southeast Imports (DSEI)
12/29/2017
54FCH16LICORICE (HERBAL & BOTANICALS, NOT TEAS)
3863PLANT PART
3864NCONTACT
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is JAIRAMDASS KHUSHIRAM's FDA import refusal history?

JAIRAMDASS KHUSHIRAM (FEI: 3012742822) has 10 FDA import refusal record(s) in our database, spanning from 12/29/2017 to 12/29/2017.

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. JAIRAMDASS KHUSHIRAM's FEI number is 3012742822.

What types of violations has JAIRAMDASS KHUSHIRAM received?

JAIRAMDASS KHUSHIRAM 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 JAIRAMDASS KHUSHIRAM come from?

All FDA import refusal data for JAIRAMDASS KHUSHIRAM 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.