Pujiang Freezing Factory of Xiamen Xiangan
FDA import alert and refusal historyXiamen, ChinaFEI 3004257170
Recorded by FDA as PUJIANG FREEZING FACTORY OF XIAMEN XIANGAN
As of October 27, 2026, Pujiang Freezing Factory of Xiamen Xiangan (Xiamen, China) is on the red list of FDA Import Alert 16-127 (Seafood: chloramphenicol) for frog legs, published by FDA on October 17, 2024, is also listed on Import Alert 16-124 (red list) and Import Alert 16-81 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Pujiang Freezing Factory of Xiamen Xiangan
3 records, newest first. Each line links to the FDA page it came from.
2024
- Import alert listingListed on Import Alert 16-127red listFrog LegsSource
2011
- Import alert listingListed on Import Alert 16-124red listFrog LegsSource
2009
- Import alert listingListed on Import Alert 16-81red listFrozen Yellow CroakerSource
Questions about Pujiang Freezing Factory of Xiamen Xiangan
- Is Pujiang Freezing Factory of Xiamen Xiangan on an FDA import alert?
- Yes. As of October 27, 2026, Pujiang Freezing Factory of Xiamen Xiangan is on the red list of FDA Import Alert 16-127, “Seafood: chloramphenicol”, for frog legs; FDA published the listing on October 17, 2024.
- Has FDA refused shipments from Pujiang Freezing Factory of Xiamen Xiangan?
- No FDA import refusals for Pujiang Freezing Factory of Xiamen Xiangan appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Pujiang Freezing Factory of Xiamen Xiangan's FEI number?
- Pujiang Freezing Factory of Xiamen Xiangan's FDA Establishment Identifier (FEI) is 3004257170.
- Can shipments from Pujiang Freezing Factory of Xiamen Xiangan still enter the U.S.?
- Shipments of frog legs from Pujiang Freezing Factory of Xiamen Xiangan can be detained without physical examination under Import Alert 16-127; 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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