Znova Agroindustrias Spr de RL de CV
FDA import alert and refusal historyMerida, MexicoFEI 3010741176
Recorded by FDA as ZNOVA AGROINDUSTRIAS SPR DE RL DE CV
As of October 26, 2026, Znova Agroindustrias Spr de RL de CV (Merida, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for habanero peppers, published by FDA on December 18, 2015, is also listed on Import Alert 21-17 (green list), 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 21-17 · green listIA 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 Znova Agroindustrias Spr de RL de CV
2 records, newest first. Each line links to the FDA page it came from.
2016
- Import alert listingListed on Import Alert 21-17green listPapayasSource
2015
- Import alert listingListed on Import Alert 99-05red listHabanero PeppersSource
Questions about Znova Agroindustrias Spr de RL de CV
- Is Znova Agroindustrias Spr de RL de CV on an FDA import alert?
- Yes. As of October 26, 2026, Znova Agroindustrias Spr de RL de CV is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for habanero peppers; FDA published the listing on December 18, 2015.
- Has FDA refused shipments from Znova Agroindustrias Spr de RL de CV?
- No FDA import refusals for Znova Agroindustrias Spr de RL de CV appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Znova Agroindustrias Spr de RL de CV's FEI number?
- Znova Agroindustrias Spr de RL de CV's FDA Establishment Identifier (FEI) is 3010741176.
- Can shipments from Znova Agroindustrias Spr de RL de CV still enter the U.S.?
- Shipments of habanero peppers from Znova Agroindustrias Spr de RL de CV 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.