Zhongshan Zhongjing Import & Export Co. Ltd.
FDA import alert and refusal historyZhongshan, ChinaFEI 3005169501
Recorded by FDA as ZHONGSHAN ZHONGJING IMPORT & EXPORT CO. LTD.
As of October 26, 2026, Zhongshan Zhongjing Import & Export Co. Ltd. (Zhongshan, China) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for mussels; dried mussels, published by FDA on September 18, 2009, is also listed on Import Alert 99-19 (red list), 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 16-81 · red listIA 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Zhongshan Zhongjing Import & Export Co. Ltd.
2 records, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-81red listMussels; Dried musselsSource
- Import alert listingListed on Import Alert 99-19red listblack sesame seedSource
Questions about Zhongshan Zhongjing Import & Export Co. Ltd.
- Is Zhongshan Zhongjing Import & Export Co. Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Zhongshan Zhongjing Import & Export Co. Ltd. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for mussels; dried mussels; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Zhongshan Zhongjing Import & Export Co. Ltd.?
- No FDA import refusals for Zhongshan Zhongjing Import & Export Co. Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Zhongshan Zhongjing Import & Export Co. Ltd.'s FEI number?
- Zhongshan Zhongjing Import & Export Co. Ltd.'s FDA Establishment Identifier (FEI) is 3005169501.
- Can shipments from Zhongshan Zhongjing Import & Export Co. Ltd. still enter the U.S.?
- Shipments of mussels; dried mussels from Zhongshan Zhongjing Import & Export Co. Ltd. can be detained without physical examination under Import Alert 16-81; 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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