Pimursa S.L.
FDA import alert and refusal historyMurcia, SpainFEI 3011304254
Recorded by FDA as PIMURSA S.L.
As of October 26, 2026, Pimursa S.L. (Murcia, Spain) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for thyme, published by FDA on December 21, 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 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Pimursa S.L.
2 records, newest first. Each line links to the FDA page it came from.
2018
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2011
- Import alert listingListed on Import Alert 99-19red listThymeSource
Questions about Pimursa S.L.
- Is Pimursa S.L. on an FDA import alert?
- Yes. As of October 26, 2026, Pimursa S.L. is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for thyme; FDA published the listing on December 21, 2011.
- Has FDA refused shipments from Pimursa S.L.?
- No FDA import refusals for Pimursa S.L. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Pimursa S.L. last inspected by FDA?
- FDA's most recent inspection of Pimursa S.L. with a final classification is dated June 8, 2018 and was classified NAI (No Action Indicated).
- What is Pimursa S.L.'s FEI number?
- Pimursa S.L.'s FDA Establishment Identifier (FEI) is 3011304254.
- Can shipments from Pimursa S.L. still enter the U.S.?
- Shipments of thyme from Pimursa S.L. 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).
Buying from Pimursa S.L.?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.