Garden Valley Export Corporation
FDA import alert and refusal historyAlagianallur, IndiaFEI 3003265350
As of October 26, 2026, Garden Valley Export Corporation (Alagianallur, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for red chili pepper ground, published by FDA on June 23, 2010, 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 99-19 · 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 Garden Valley Export Corporation
2 records, newest first. Each line links to the FDA page it came from.
2011
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2010
- Import alert listingListed on Import Alert 99-19red listRed Chili Pepper GroundSource
Questions about Garden Valley Export Corporation
- Is Garden Valley Export Corporation on an FDA import alert?
- Yes. As of October 26, 2026, Garden Valley Export Corporation is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for red chili pepper ground; FDA published the listing on June 23, 2010.
- Has FDA refused shipments from Garden Valley Export Corporation?
- No FDA import refusals for Garden Valley Export Corporation appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Garden Valley Export Corporation last inspected by FDA?
- FDA's most recent inspection of Garden Valley Export Corporation with a final classification is dated August 25, 2011 and was classified VAI (Voluntary Action Indicated).
- What is Garden Valley Export Corporation's FEI number?
- Garden Valley Export Corporation's FDA Establishment Identifier (FEI) is 3003265350.
- Can shipments from Garden Valley Export Corporation still enter the U.S.?
- Shipments of red chili pepper ground from Garden Valley Export Corporation can be detained without physical examination under Import Alert 99-19; 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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