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Rangoon Chemical Works, PVT. LTD.

⚠️ Moderate Risk

FEI: 3005162154 • Gujarat • INDIA

FEI

FEI Number

3005162154

📍

Location

Gujarat

🇮🇳

Country

INDIA
🏢

Address

Plot 238, Masma 394 540 Dist. Surat, Gujarat, , India

Moderate Risk

FDA Import Risk Assessment

33.6
LowModerateHighCritical

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

Statistics

5
Total Refusals
10
Unique Violations
9/13/2016
Latest Refusal
7/9/2005
Earliest Refusal

Score Breakdown

Violation Severity
61.4×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
4.5×10%
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

1184×

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).

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).

3303×

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).

4833×

DRUG NAME

The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.

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.

162×

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.

1782×

COL ADDED

The article appears to bear or contain, for the purpose of coloring only, a color additive which is unsafe within the meaning of Section 721(a).

3241×

NO ENGLISH

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

4731×

LABELING

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

2181×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

Refusal History

DateProductViolationsDivision
9/13/2016
65SBJ99RUBEFACIENT N.E.C.
118NOT LISTED
16DIRECTIONS
178COL ADDED
3280FRNMFGREG
330UNSAFE COL
483DRUG NAME
75UNAPPROVED
Division of Northeast Imports (DNEI)
9/13/2016
65SBJ99RUBEFACIENT N.E.C.
118NOT LISTED
16DIRECTIONS
178COL ADDED
3280FRNMFGREG
330UNSAFE COL
483DRUG NAME
75UNAPPROVED
Division of Northeast Imports (DNEI)
6/12/2013
54FEJ99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
324NO ENGLISH
473LABELING
Southwest Import District Office (SWI-DO)
1/5/2011
60LBJ99ANALGESIC, N.E.C.
118NOT LISTED
330UNSAFE COL
75UNAPPROVED
New York District Office (NYK-DO)
7/9/2005
60LBJ63SALICYLAMIDE (ANALGESIC)
118NOT LISTED
483DRUG NAME
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Rangoon Chemical Works, PVT. LTD.'s FDA import refusal history?

Rangoon Chemical Works, PVT. LTD. (FEI: 3005162154) has 5 FDA import refusal record(s) in our database, spanning from 7/9/2005 to 9/13/2016.

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. Rangoon Chemical Works, PVT. LTD.'s FEI number is 3005162154.

What types of violations has Rangoon Chemical Works, PVT. LTD. received?

Rangoon Chemical Works, PVT. LTD. has been cited for 10 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 Rangoon Chemical Works, PVT. LTD. come from?

All FDA import refusal data for Rangoon Chemical Works, PVT. 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.