Columba Robin
FDA import alert and refusal historyPimampiro, EcuadorFEI 3005573175
As of October 25, 2026, Columba Robin (Pimampiro, Ecuador) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for pepinos (subtropical and tropical fruits), raw, fresh, ambient; pepinos (subtropical and tropical fruits), raw, fresh, refrigerated, published by FDA on September 16, 2009, 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 99-05 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Columba Robin
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listPepinos (Subtropical and Tropical Fruits), Raw, Fresh, Ambient; Pepinos (Subtropical and Tropical Fruits), Raw, Fresh, RefrigeratedSource
Questions about Columba Robin
- Is Columba Robin on an FDA import alert?
- Yes. As of October 25, 2026, Columba Robin is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for pepinos (subtropical and tropical fruits), raw, fresh, ambient; pepinos (subtropical and tropical fruits), raw, fresh, refrigerated; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Columba Robin?
- No FDA import refusals for Columba Robin appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Columba Robin's FEI number?
- Columba Robin's FDA Establishment Identifier (FEI) is 3005573175.
- Can shipments from Columba Robin still enter the U.S.?
- Shipments of pepinos (subtropical and tropical fruits), raw, fresh, ambient; pepinos (subtropical and tropical fruits), raw, fresh, refrigerated from Columba Robin can be detained without physical examination under Import Alert 99-05; 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.