Promarisco S.A.
FDA import alert and refusal historyGuayaquil, EcuadorFEI 3009908739
Recorded by FDA as PROMARISCO S.A.
As of October 25, 2026, Promarisco S.A. (Guayaquil, Ecuador) is on the red list of FDA Import Alert 99-37 (Low-acid canned/acidified foods without scheduled process) for liquid oat drink (1 liter only), published by FDA on January 14, 2016, 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 99-37 · 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 Promarisco S.A.
2 records, newest first. Each line links to the FDA page it came from.
2016
- Import alert listingListed on Import Alert 99-37red listLiquid Oat Drink (1 Liter only)Source
2014
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Promarisco S.A.
- Is Promarisco S.A. on an FDA import alert?
- Yes. As of October 25, 2026, Promarisco S.A. is on the red list of FDA Import Alert 99-37, “Low-acid canned/acidified foods without scheduled process”, for liquid oat drink (1 liter only); FDA published the listing on January 14, 2016.
- Has FDA refused shipments from Promarisco S.A.?
- No FDA import refusals for Promarisco S.A. appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Promarisco S.A. last inspected by FDA?
- FDA's most recent inspection of Promarisco S.A. with a final classification is dated June 11, 2014 and was classified VAI (Voluntary Action Indicated).
- What is Promarisco S.A.'s FEI number?
- Promarisco S.A.'s FDA Establishment Identifier (FEI) is 3009908739.
- Can shipments from Promarisco S.A. still enter the U.S.?
- Shipments of liquid oat drink (1 liter only) from Promarisco S.A. can be detained without physical examination under Import Alert 99-37; 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.