Inversiones Mejia S de RL
FDA import alert and refusal historyComayagua, HondurasFEI 3004249282
Recorded by FDA as INVERSIONES MEJIA S DE RL
As of October 26, 2026, Inversiones Mejia S de RL (Comayagua, Honduras) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for chinese eggplanct; chinese eggplant, published by FDA on October 30, 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
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Inversiones Mejia S de RL
2 records, newest first. Each line links to the FDA page it came from.
2010
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 99-05red listChinese Eggplanct; Chinese EggplantSource
Questions about Inversiones Mejia S de RL
- Is Inversiones Mejia S de RL on an FDA import alert?
- Yes. As of October 26, 2026, Inversiones Mejia S de RL is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for chinese eggplanct; chinese eggplant; FDA published the listing on October 30, 2009.
- Has FDA refused shipments from Inversiones Mejia S de RL?
- No FDA import refusals for Inversiones Mejia S de RL appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Inversiones Mejia S de RL last inspected by FDA?
- FDA's most recent inspection of Inversiones Mejia S de RL with a final classification is dated December 2, 2010 and was classified VAI (Voluntary Action Indicated).
- What is Inversiones Mejia S de RL's FEI number?
- Inversiones Mejia S de RL's FDA Establishment Identifier (FEI) is 3004249282.
- Can shipments from Inversiones Mejia S de RL still enter the U.S.?
- Shipments of chinese eggplanct; chinese eggplant from Inversiones Mejia S de RL 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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