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Raptakos, Brett & Co. Ltd.

⚠️ Moderate Risk

FEI: 3002926082 • Mumbai, Maharashtra • INDIA

FEI

FEI Number

3002926082

📍

Location

Mumbai, Maharashtra

🇮🇳

Country

INDIA
🏢

Address

Dr Annie Besant Road, , Mumbai, Maharashtra, India

Moderate Risk

FDA Import Risk Assessment

48.2
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
7/2/2025
Latest Refusal
6/24/2025
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
17.7×30%
Recency
74.6×20%
Frequency
20.0×10%
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

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

751×

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
7/2/2025
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/24/2025
41BET99FOODS WITH SUPPLEMENTAL NUTRIENTS ADDED, WITH OR WITHOUT ARTIFICAL SWEETNERS
473LABELING
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Raptakos, Brett & Co. Ltd.'s FDA import refusal history?

Raptakos, Brett & Co. Ltd. (FEI: 3002926082) has 2 FDA import refusal record(s) in our database, spanning from 6/24/2025 to 7/2/2025.

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. Raptakos, Brett & Co. Ltd.'s FEI number is 3002926082.

What types of violations has Raptakos, Brett & Co. Ltd. received?

Raptakos, Brett & Co. Ltd. has been cited for 2 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 Raptakos, Brett & Co. Ltd. come from?

All FDA import refusal data for Raptakos, Brett & Co. Ltd. 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.