Synthite (Dezhou) Biotech Co., Ltd.
FDA import alert and refusal historyDezhou, ChinaFEI 3015346688
As of October 26, 2026, Synthite (Dezhou) Biotech Co., Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between January 28, 2025 and April 1, 2025, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Paprika, ground, cracked (spice) · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Synthite (Dezhou) Biotech Co., Ltd.
3 records, newest first. Each line links to the FDA page it came from.
2026
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2025
Refusal charges, in plain English
- FILTHY2 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Synthite (Dezhou) Biotech Co., Ltd.
- Is Synthite (Dezhou) Biotech Co., Ltd. on an FDA import alert?
- No listing for Synthite (Dezhou) Biotech Co., Ltd. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the China page.
- Has FDA refused shipments from Synthite (Dezhou) Biotech Co., Ltd.?
- Yes. FDA refused 2 shipment lines from Synthite (Dezhou) Biotech Co., Ltd. between January 28, 2025 and April 1, 2025. The most recent, on April 1, 2025, was paprika, ground, cracked (spice), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Synthite (Dezhou) Biotech Co., Ltd.'s shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
- When was Synthite (Dezhou) Biotech Co., Ltd. last inspected by FDA?
- FDA's most recent inspection of Synthite (Dezhou) Biotech Co., Ltd. with a final classification is dated February 5, 2026 and was classified VAI (Voluntary Action Indicated).
- What is Synthite (Dezhou) Biotech Co., Ltd.'s FEI number?
- Synthite (Dezhou) Biotech Co., Ltd.'s FDA Establishment Identifier (FEI) is 3015346688.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.