LABORATORY QP PHARMACHEM LIMITED
⚠️ High Risk
FEI: 3031224065 • Dera • INDIA
FEI Number
3031224065
Location
Dera
Country
INDIAAddress
F5, Industrial Land Zon, , Said He Majra, Dera, , India
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
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
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).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/2/2024 | 66JCY02LIOTHYRONINE SODIUM (THYROID HORMONE) | Division of Southeast Imports (DSEI) | |
| 7/2/2024 | 64RDY17ANASTROZOLE (HORMONE) | Division of Southeast Imports (DSEI) | |
| 7/2/2024 | 60NCY15TESTOSTERONE CYPIONATE (ANDROGEN) | Division of Southeast Imports (DSEI) | |
| 7/2/2024 | 63BCY35CLENBUTEROL (BRONCHODILATOR) | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is LABORATORY QP PHARMACHEM LIMITED's FDA import refusal history?
LABORATORY QP PHARMACHEM LIMITED (FEI: 3031224065) has 4 FDA import refusal record(s) in our database, spanning from 7/2/2024 to 7/2/2024.
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. LABORATORY QP PHARMACHEM LIMITED's FEI number is 3031224065.
What types of violations has LABORATORY QP PHARMACHEM LIMITED received?
LABORATORY QP PHARMACHEM LIMITED 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 LABORATORY QP PHARMACHEM LIMITED come from?
All FDA import refusal data for LABORATORY QP PHARMACHEM 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.