Shandong Zhonglu Food Co Ltd
FDA import alert and refusal historyJu County, ChinaFEI 3004347997
As of October 26, 2026, Shandong Zhonglu Food Co Ltd (Ju County, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for peapods; mixed peppers, published by FDA on February 23, 2012, 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 Shandong Zhonglu Food Co Ltd
2 records, newest first. Each line links to the FDA page it came from.
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2012
- Import alert listingListed on Import Alert 99-08red listPeapods; Mixed PeppersSource
Questions about Shandong Zhonglu Food Co Ltd
- Is Shandong Zhonglu Food Co Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Shandong Zhonglu Food Co Ltd is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for peapods; mixed peppers; FDA published the listing on February 23, 2012.
- Has FDA refused shipments from Shandong Zhonglu Food Co Ltd?
- No FDA import refusals for Shandong Zhonglu Food Co Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Shandong Zhonglu Food Co Ltd last inspected by FDA?
- FDA's most recent inspection of Shandong Zhonglu Food Co Ltd with a final classification is dated August 25, 2016 and was classified VAI (Voluntary Action Indicated).
- What is Shandong Zhonglu Food Co Ltd's FEI number?
- Shandong Zhonglu Food Co Ltd's FDA Establishment Identifier (FEI) is 3004347997.
- Can shipments from Shandong Zhonglu Food Co Ltd still enter the U.S.?
- Shipments of peapods; mixed peppers from Shandong Zhonglu Food 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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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.