Proinca S.A. De C.V.
FDA import alert and refusal historySan Salvador, El SalvadorFEI 1000326582
As of October 26, 2026, Proinca S.A. De C.V. (San Salvador, El Salvador) is on the red list of FDA Import Alert 23-14 (Food products: mycotoxins) for pumpkin seeds; pumpkin seeds & pumpkin flour, published by FDA on February 3, 2011, 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 23-14 · 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 Proinca S.A. De C.V.
2 records, newest first. Each line links to the FDA page it came from.
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2011
- Import alert listingListed on Import Alert 23-14red listPumpkin Seeds; Pumpkin Seeds & Pumpkin FlourSource
Questions about Proinca S.A. De C.V.
- Is Proinca S.A. De C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Proinca S.A. De C.V. is on the red list of FDA Import Alert 23-14, “Food products: mycotoxins”, for pumpkin seeds; pumpkin seeds & pumpkin flour; FDA published the listing on February 3, 2011.
- Has FDA refused shipments from Proinca S.A. De C.V.?
- No FDA import refusals for Proinca S.A. De C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Proinca S.A. De C.V. last inspected by FDA?
- FDA's most recent inspection of Proinca S.A. De C.V. with a final classification is dated July 26, 2016 and was classified VAI (Voluntary Action Indicated).
- What is Proinca S.A. De C.V.'s FEI number?
- Proinca S.A. De C.V.'s FDA Establishment Identifier (FEI) is 1000326582.
- Can shipments from Proinca S.A. De C.V. still enter the U.S.?
- Shipments of pumpkin seeds; pumpkin seeds & pumpkin flour from Proinca S.A. De C.V. can be detained without physical examination under Import Alert 23-14; 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.