M.S. Export C.X.A
FDA import alert and refusal historyLa Vega, Dominican RepublicFEI 2000017968
As of October 25, 2026, M.S. Export C.X.A (La Vega, Dominican Republic) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for fresh indian long squash, published by FDA on January 2, 2014, 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 99-23 · 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 M.S. Export C.X.A
2 records, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-23red listFresh Indian Long SquashSource
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about M.S. Export C.X.A
- Is M.S. Export C.X.A on an FDA import alert?
- Yes. As of October 25, 2026, M.S. Export C.X.A is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for fresh indian long squash; FDA published the listing on January 2, 2014.
- Has FDA refused shipments from M.S. Export C.X.A?
- No FDA import refusals for M.S. Export C.X.A appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was M.S. Export C.X.A last inspected by FDA?
- FDA's most recent inspection of M.S. Export C.X.A with a final classification is dated December 8, 2012 and was classified VAI (Voluntary Action Indicated).
- What is M.S. Export C.X.A's FEI number?
- M.S. Export C.X.A's FDA Establishment Identifier (FEI) is 2000017968.
- Can shipments from M.S. Export C.X.A still enter the U.S.?
- Shipments of fresh indian long squash from M.S. Export C.X.A can be detained without physical examination under Import Alert 99-23; 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.