Fujian Dragon Enterprises Co., Ltd
FDA import alert and refusal historyFuzhou City, ChinaFEI 1000140963
As of October 26, 2026, Fujian Dragon Enterprises Co., Ltd (Fuzhou City, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for iqf chinese pea pods; iqf sugar snap peas; sugar snap peas, raw - fresh, frozen, natural state, published by FDA on September 16, 2009, 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
- None on record
Every FDA record for Fujian Dragon Enterprises Co., Ltd
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-08red listIQF Chinese Pea Pods; IQF sugar snap peas; Sugar Snap Peas, Raw - Fresh, Frozen, Natural StateSource
Questions about Fujian Dragon Enterprises Co., Ltd
- Is Fujian Dragon Enterprises Co., Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Fujian Dragon Enterprises Co., Ltd is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for iqf chinese pea pods; iqf sugar snap peas; sugar snap peas, raw - fresh, frozen, natural state; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Fujian Dragon Enterprises Co., Ltd?
- No FDA import refusals for Fujian Dragon Enterprises Co., Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Fujian Dragon Enterprises Co., Ltd's FEI number?
- Fujian Dragon Enterprises Co., Ltd's FDA Establishment Identifier (FEI) is 1000140963.
- Can shipments from Fujian Dragon Enterprises Co., Ltd still enter the U.S.?
- Shipments of iqf chinese pea pods; iqf sugar snap peas; sugar snap peas, raw - fresh, frozen, natural state from Fujian Dragon Enterprises Co., Ltd 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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