Interagra Sh.P.K.Export Botanical & Aromatic Pl
FDA import alert and refusal historyKurbin, AlbaniaFEI 3003448076
As of October 26, 2026, Interagra Sh.P.K.Export Botanical & Aromatic Pl (Kurbin, Albania) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for sage, whole (spice); sage, ground, cracked (spice), 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 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Interagra Sh.P.K.Export Botanical & Aromatic Pl
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-19red listSage, Whole (Spice); Sage, Ground, Cracked (Spice)Source
Questions about Interagra Sh.P.K.Export Botanical & Aromatic Pl
- Is Interagra Sh.P.K.Export Botanical & Aromatic Pl on an FDA import alert?
- Yes. As of October 26, 2026, Interagra Sh.P.K.Export Botanical & Aromatic Pl is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for sage, whole (spice); sage, ground, cracked (spice); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Interagra Sh.P.K.Export Botanical & Aromatic Pl?
- No FDA import refusals for Interagra Sh.P.K.Export Botanical & Aromatic Pl appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Interagra Sh.P.K.Export Botanical & Aromatic Pl's FEI number?
- Interagra Sh.P.K.Export Botanical & Aromatic Pl's FDA Establishment Identifier (FEI) is 3003448076.
- Can shipments from Interagra Sh.P.K.Export Botanical & Aromatic Pl still enter the U.S.?
- Shipments of sage, whole (spice); sage, ground, cracked (spice) from Interagra Sh.P.K.Export Botanical & Aromatic Pl can be detained without physical examination under Import Alert 99-19; 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.