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Pts Packers And Providers Pvt Lt

⚠️ Moderate Risk

FEI: 3010291071 • Sikkim • INDIA

FEI

FEI Number

3010291071

📍

Location

Sikkim

🇮🇳

Country

INDIA
🏢

Address

Sangkohla Singtam, , Sikkim, , India

Moderate Risk

FDA Import Risk Assessment

42.5
LowModerateHighCritical

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

Statistics

7
Total Refusals
5
Unique Violations
4/29/2022
Latest Refusal
9/7/2017
Earliest Refusal

Score Breakdown

Violation Severity
71.5×40%
Refusal Volume
33.5×30%
Recency
11.6×20%
Frequency
15.1×10%
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

756×

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).

22802×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.

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.

161×

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.

Refusal History

DateProductViolationsDivision
4/29/2022
61WDJ04CLOTRIMAZOLE (ANTI-FUNGAL) (NOT ANTIBIOTIC)
118NOT LISTED
2280DIRSEXMPT
3280FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
3/3/2022
66VDJ99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Northeast Imports (DNEI)
11/17/2021
61WDJ04CLOTRIMAZOLE (ANTI-FUNGAL) (NOT ANTIBIOTIC)
75UNAPPROVED
Division of Northeast Imports (DNEI)
10/22/2021
61WDJ04CLOTRIMAZOLE (ANTI-FUNGAL) (NOT ANTIBIOTIC)
75UNAPPROVED
Division of Northeast Imports (DNEI)
8/13/2021
66VCS99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
2280DIRSEXMPT
3280FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
7/2/2018
61WBO04CLOTRIMAZOLE (ANTI-FUNGAL) (NOT ANTIBIOTIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/7/2017
61WDJ04CLOTRIMAZOLE (ANTI-FUNGAL) (NOT ANTIBIOTIC)
16DIRECTIONS
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Pts Packers And Providers Pvt Lt's FDA import refusal history?

Pts Packers And Providers Pvt Lt (FEI: 3010291071) has 7 FDA import refusal record(s) in our database, spanning from 9/7/2017 to 4/29/2022.

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. Pts Packers And Providers Pvt Lt's FEI number is 3010291071.

What types of violations has Pts Packers And Providers Pvt Lt received?

Pts Packers And Providers Pvt Lt 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 Pts Packers And Providers Pvt Lt come from?

All FDA import refusal data for Pts Packers And Providers Pvt Lt 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.