Zhenjiang Mouferry Food Co.,Ltd.
FDA import alert and refusal historyJiangsu, ChinaFEI 3014512567
Recorded by FDA as ZHENJIANG MOUFERRY FOOD CO.,LTD.
As of October 26, 2026, Zhenjiang Mouferry Food Co.,Ltd. (Jiangsu, China) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for ready-to-eat (rte) fermented fish sauce in pet plastic bottles or pe plastic bags in cartons, published by FDA on May 19, 2026, 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 16-120 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Zhenjiang Mouferry Food Co.,Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 16-120red listReady-to-Eat (RTE) Fermented Fish Sauce in PET plastic bottles or PE plastic bags in cartonsSource
Questions about Zhenjiang Mouferry Food Co.,Ltd.
- Is Zhenjiang Mouferry Food Co.,Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Zhenjiang Mouferry Food Co.,Ltd. is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for ready-to-eat (rte) fermented fish sauce in pet plastic bottles or pe plastic bags in cartons; FDA published the listing on May 19, 2026.
- Has FDA refused shipments from Zhenjiang Mouferry Food Co.,Ltd.?
- No FDA import refusals for Zhenjiang Mouferry Food Co.,Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Zhenjiang Mouferry Food Co.,Ltd.'s FEI number?
- Zhenjiang Mouferry Food Co.,Ltd.'s FDA Establishment Identifier (FEI) is 3014512567.
- Can shipments from Zhenjiang Mouferry Food Co.,Ltd. still enter the U.S.?
- Shipments of ready-to-eat (rte) fermented fish sauce in pet plastic bottles or pe plastic bags in cartons from Zhenjiang Mouferry Food Co.,Ltd. can be detained without physical examination under Import Alert 16-120; 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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