Proyimar S.A.
FDA import alert and refusal historyGuayaquil, EcuadorFEI 3010144231
As of October 26, 2026, Proyimar 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 22, 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 Proyimar 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)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Proyimar S.A.
- Is Proyimar S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Proyimar 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 22, 2016.
- Has FDA refused shipments from Proyimar S.A.?
- No FDA import refusals for Proyimar S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Proyimar S.A. last inspected by FDA?
- FDA's most recent inspection of Proyimar S.A. with a final classification is dated June 13, 2014 and was classified VAI (Voluntary Action Indicated).
- What is Proyimar S.A.'s FEI number?
- Proyimar S.A.'s FDA Establishment Identifier (FEI) is 3010144231.
- Can shipments from Proyimar S.A. still enter the U.S.?
- Shipments of liquid oat drink (1 liter only) from Proyimar 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.