The ACME Laboratories Ltd.
⚠️ High Risk
FEI: 3013354357 • Dhaka • BANGLADESH
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
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).
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/10/2025 | 54FEY94ASHWAGANDHA (HERBAL & BOTANICALS, NOT TEAS) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 6/3/2025 | 66VDY99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 11/22/2024 | 62ICB14CIROLEMYCIN (ANTI-NEOPLASTIC) | 75UNAPPROVED | Division of West Coast Imports (DWCI) |
| 10/3/2023 | 62OCY22CARVEDILOL (ANTI-HYPERTENSIVE - PART II) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 10/3/2023 | 62OCY37IRBESARTAN (ANTI-HYPERTENSIVE - PART II) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 7/6/2020 | 61JCB09FENOFIBRATE (ANTI-CHOLESTEREMIC) | 118NOT LISTED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is The ACME Laboratories Ltd.'s FDA import refusal history?
The ACME Laboratories Ltd. (FEI: 3013354357) has 6 FDA import refusal record(s) in our database, spanning from 7/6/2020 to 11/10/2025.
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. The ACME Laboratories Ltd.'s FEI number is 3013354357.
What types of violations has The ACME Laboratories Ltd. received?
The ACME Laboratories 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 The ACME Laboratories Ltd. come from?
All FDA import refusal data for The ACME Laboratories 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.