Runbio Biotech Co., Ltd.
✅ Low Risk
FEI: 3005216656 • Shantou, Guangdong • CHINA
FEI Number
3005216656
Location
Shantou, Guangdong
Country
CHINAAddress
University Road, Rongsheng Technological Zone, Shantou, Guangdong, China
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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).
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
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.
LACKS FIRM
The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/7/2013 | 75LCXKIT, TEST, PREGNANCY, HCG, OVER THE COUNTER | Division of Northeast Imports (DNEI) | |
| 10/19/2006 | 75LCXKIT, TEST, PREGNANCY, HCG, OVER THE COUNTER | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is Runbio Biotech Co., Ltd.'s FDA import refusal history?
Runbio Biotech Co., Ltd. (FEI: 3005216656) has 2 FDA import refusal record(s) in our database, spanning from 10/19/2006 to 3/7/2013.
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. Runbio Biotech Co., Ltd.'s FEI number is 3005216656.
What types of violations has Runbio Biotech Co., Ltd. received?
Runbio Biotech Co., Ltd. has been cited for 6 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 Runbio Biotech Co., Ltd. come from?
All FDA import refusal data for Runbio Biotech Co., 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.