Panion & BF Biotech Inc.
⚠️ Moderate Risk
FEI: 3015652009 • New Taipei City • TAIWAN
FEI Number
3015652009
Location
New Taipei City
Country
TAIWANAddress
Xizhi District, No. 308-8 Datong Rd, Sec. 1, New Taipei City, , Taiwan
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
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).
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/9/2022 | 83GPDANTIGEN, INDIRECT FLUORESCENT ANTIBODY TEST, ECHINOCOCCUS GRANULOSUS | Division of Southeast Imports (DSEI) | |
| 11/1/2021 | 57VL99IN-VITRO DIAG PRODUCTS, N.E.C. | Division of West Coast Imports (DWCI) | |
| 4/12/2021 | 83QJRREAGENTS, 2019-NOVEL CORONAVIRUS NUCLEIC ACID | Division of Southeast Imports (DSEI) | |
| 10/16/2020 | 83QKPCORONAVIRUS ANTIGEN DETECTION TEST SYSTEM. | 508NO 510(K) | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Panion & BF Biotech Inc.'s FDA import refusal history?
Panion & BF Biotech Inc. (FEI: 3015652009) has 4 FDA import refusal record(s) in our database, spanning from 10/16/2020 to 2/9/2022.
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. Panion & BF Biotech Inc.'s FEI number is 3015652009.
What types of violations has Panion & BF Biotech Inc. received?
Panion & BF Biotech Inc. has been cited for 4 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 Panion & BF Biotech Inc. come from?
All FDA import refusal data for Panion & BF Biotech Inc. 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.