Sunwoofarm
⚠️ Moderate Risk
FEI: 3021939362 • Jinju, Gyeongsangnamdo • SOUTH KOREA
FEI Number
3021939362
Location
Jinju, Gyeongsangnamdo
Country
SOUTH KOREAAddress
437-8 Dongbu-Ro, Munsan-Eup, Jinju, Gyeongsangnamdo, South Korea
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
FSVP VIO
The article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) in that it appears that the importer (as defined in section 805 of the FD&C Act) is in violation of section 805.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/6/2023 | 25PGC04MUSHROOM, SHIITAKE , WHOLE (BUTTON) (FUNGI) | 3886FSVP VIO | Division of West Coast Imports (DWCI) |
| 1/6/2023 | 25PGC11ENOKITAKE MUSHROOMS, WHOLE (BUTTON) (FUNGI) | 3886FSVP VIO | Division of West Coast Imports (DWCI) |
| 7/15/2022 | 25PGC04MUSHROOM, SHIITAKE , WHOLE (BUTTON) (FUNGI) | 3886FSVP VIO | Division of West Coast Imports (DWCI) |
| 7/15/2022 | 25PGC04MUSHROOM, SHIITAKE , WHOLE (BUTTON) (FUNGI) | 3886FSVP VIO | Division of West Coast Imports (DWCI) |
| 7/15/2022 | 25PGC04MUSHROOM, SHIITAKE , WHOLE (BUTTON) (FUNGI) | 3886FSVP VIO | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is Sunwoofarm's FDA import refusal history?
Sunwoofarm (FEI: 3021939362) has 5 FDA import refusal record(s) in our database, spanning from 7/15/2022 to 1/6/2023.
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. Sunwoofarm's FEI number is 3021939362.
What types of violations has Sunwoofarm received?
Sunwoofarm has been cited for 1 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 Sunwoofarm come from?
All FDA import refusal data for Sunwoofarm 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.