WSSF Corporation ( Weifang )
FDA import alert and refusal historyWeifang, ChinaFEI 2000039361
As of October 26, 2026, WSSF Corporation ( Weifang ) (Weifang, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for frozen shitake mushrooms, published by FDA on July 21, 2014, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for WSSF Corporation ( Weifang )
2 records, newest first. Each line links to the FDA page it came from.
2015
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2014
- Import alert listingListed on Import Alert 99-08red listFrozen Shitake MushroomsSource
Questions about WSSF Corporation ( Weifang )
- Is WSSF Corporation ( Weifang ) on an FDA import alert?
- Yes. As of October 26, 2026, WSSF Corporation ( Weifang ) is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for frozen shitake mushrooms; FDA published the listing on July 21, 2014.
- Has FDA refused shipments from WSSF Corporation ( Weifang )?
- No FDA import refusals for WSSF Corporation ( Weifang ) appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was WSSF Corporation ( Weifang ) last inspected by FDA?
- FDA's most recent inspection of WSSF Corporation ( Weifang ) with a final classification is dated June 25, 2015 and was classified VAI (Voluntary Action Indicated).
- What is WSSF Corporation ( Weifang )'s FEI number?
- WSSF Corporation ( Weifang )'s FDA Establishment Identifier (FEI) is 2000039361.
- Can shipments from WSSF Corporation ( Weifang ) still enter the U.S.?
- Shipments of frozen shitake mushrooms from WSSF Corporation ( Weifang ) can be detained without physical examination under Import Alert 99-08; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.