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Pfizer Limited

⚠️ High Risk

FEI: 3012205767 • Goa • INDIA

FEI

FEI Number

3012205767

📍

Location

Goa

🇮🇳

Country

INDIA
🏢

Address

Plot L-137 Phase 3 Averna Indust, , Goa, , India

High Risk

FDA Import Risk Assessment

57.3
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

8
Total Refusals
1
Unique Violations
2/5/2024
Latest Refusal
1/17/2018
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
35.3×30%
Recency
47.1×20%
Frequency
13.2×10%
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

758×

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
2/5/2024
64LDY50PREDNISOLONE (GLUCOCORTICOID)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/29/2023
61KCA52TRIHEXYPHENIDYL HCL (ANTI-CHOLINERGIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/15/2021
64LDA50PREDNISOLONE (GLUCOCORTICOID)
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/19/2021
54YGY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/24/2020
66MCA86LORAZEPAM (TRANQUILIZER)
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/4/2020
66VCA99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/20/2018
64GCY19ETHINYL ESTRADIOL (ESTROGEN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/17/2018
64LDB50PREDNISOLONE (GLUCOCORTICOID)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Pfizer Limited's FDA import refusal history?

Pfizer Limited (FEI: 3012205767) has 8 FDA import refusal record(s) in our database, spanning from 1/17/2018 to 2/5/2024.

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. Pfizer Limited's FEI number is 3012205767.

What types of violations has Pfizer Limited received?

Pfizer Limited has been cited for 1 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 Pfizer Limited come from?

All FDA import refusal data for Pfizer Limited 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.