Arnime, S.A. de C.V.
FDA import alert and refusal historyCelaya, MexicoFEI 3011312137
As of October 26, 2026, Arnime, S.A. de C.V. (Celaya, Mexico) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for celery stalk/leaf dried, published by FDA on April 10, 2015, 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 99-08 · 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 Arnime, S.A. de C.V.
2 records, newest first. Each line links to the FDA page it came from.
2015
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
- Import alert listingListed on Import Alert 99-08red listCelery Stalk/Leaf DriedSource
Questions about Arnime, S.A. de C.V.
- Is Arnime, S.A. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Arnime, S.A. de C.V. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for celery stalk/leaf dried; FDA published the listing on April 10, 2015.
- Has FDA refused shipments from Arnime, S.A. de C.V.?
- No FDA import refusals for Arnime, S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Arnime, S.A. de C.V. last inspected by FDA?
- FDA's most recent inspection of Arnime, S.A. de C.V. with a final classification is dated April 17, 2015 and was classified VAI (Voluntary Action Indicated).
- What is Arnime, S.A. de C.V.'s FEI number?
- Arnime, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3011312137.
- Can shipments from Arnime, S.A. de C.V. still enter the U.S.?
- Shipments of celery stalk/leaf dried from Arnime, S.A. de C.V. can be detained without physical examination under Import Alert 99-08; 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.