GODNEST BIOLOGICAL TECHNOLOGY LI
⚠️ Moderate Risk
FEI: 3012898602 • Hangzhou • CHINA
FEI Number
3012898602
Location
Hangzhou
Country
CHINAAddress
Jinjiadai Villagem Shus, , Hangzhou, , China
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
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).
NO PMA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).
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.
Refusal History
Frequently Asked Questions
What is GODNEST BIOLOGICAL TECHNOLOGY LI's FDA import refusal history?
GODNEST BIOLOGICAL TECHNOLOGY LI (FEI: 3012898602) has 1 FDA import refusal record(s) in our database, spanning from 12/1/2016 to 12/1/2016.
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. GODNEST BIOLOGICAL TECHNOLOGY LI's FEI number is 3012898602.
What types of violations has GODNEST BIOLOGICAL TECHNOLOGY LI received?
GODNEST BIOLOGICAL TECHNOLOGY LI has been cited for 3 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 GODNEST BIOLOGICAL TECHNOLOGY LI come from?
All FDA import refusal data for GODNEST BIOLOGICAL TECHNOLOGY LI 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.