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Jyothy Lab

⚠️ Moderate Risk

FEI: 3010908885 • Mumbai, Maharashtra • INDIA

FEI

FEI Number

3010908885

📍

Location

Mumbai, Maharashtra

🇮🇳

Country

INDIA
🏢

Address

Ujala House, Ram Krishna Mandir Road, Mumbai, Maharashtra, India

Moderate Risk

FDA Import Risk Assessment

49.3
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
6/10/2025
Latest Refusal
10/1/2018
Earliest Refusal

Score Breakdown

Violation Severity
65.6×40%
Refusal Volume
25.9×30%
Recency
73.4×20%
Frequency
6.0×10%
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

753×

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).

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).

32802×

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.

3301×

UNSAFE COL

The article appears to be a color additive for the purposes of coloring only in or on drugs or devices, and is unsafe within the meaning of Section 721(a).

3351×

LACKS N/C

The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.

Refusal History

DateProductViolationsDivision
6/10/2025
53IG01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS)
3280FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
4/26/2023
53IG01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS)
75UNAPPROVED
Division of West Coast Imports (DWCI)
4/30/2019
53IG01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS)
118NOT LISTED
75UNAPPROVED
Division of Northern Border Imports (DNBI)
10/1/2018
63RBJ04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC)
118NOT LISTED
3280FRNMFGREG
330UNSAFE COL
335LACKS N/C
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Jyothy Lab's FDA import refusal history?

Jyothy Lab (FEI: 3010908885) has 4 FDA import refusal record(s) in our database, spanning from 10/1/2018 to 6/10/2025.

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. Jyothy Lab's FEI number is 3010908885.

What types of violations has Jyothy Lab received?

Jyothy Lab 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 Jyothy Lab come from?

All FDA import refusal data for Jyothy Lab 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.