# Costa Rican Gold Coffee Company   DBA Gold Coffee Company, Gold Coffee Roasters,, Jupiter, FL – FDA Inspections

Source: https://www.keypedia.com/companies/costa-rican-gold-coffee-company-dba-gold-coffee-company-gold-coffee-roasters/7e3998e5-6453-4a82-9013-a5f59bf993ec

> Inspection records and compliance data for Costa Rican Gold Coffee Company   DBA Gold Coffee Company, Gold Coffee Roasters, in Jupiter, Florida. 4 FDA inspections on record, last inspected August 26, 2026.

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## Details

- Name: Costa Rican Gold Coffee Company   DBA Gold Coffee Company, Gold Coffee Roasters,
- FEI Number: 3004299983
- Address Line 1: 1425 Park Ln S
- City: Jupiter
- State: Florida
- Zip Code: 33458
- Country Name: United States
- Address: 1425 Park Ln S, Jupiter, Florida 33458, United States
- Country: United States

## Related Documents

- FDA Inspection 1334086 - Costa Rican Gold Coffee Company   DBA Gold Coffee Company, Gold Coffee Roasters, - 2026-08-26 — classification: No Action Indicated (NAI), source: FDA, date: August 26, 2026
- FDA Inspection 1259443 - Costa Rican Gold Coffee Company   DBA Gold Coffee Company, Gold Coffee Roasters, - 2024-12-13 — source: FDA, date: December 13, 2024
- FDA Inspection 1038743 - Costa Rican Gold Coffee Company   DBA Gold Coffee Company, Gold Coffee Roasters, - 2018-01-19 — source: FDA, date: January 19, 2018
- [FDA Inspection 575801 - Costa Rican Gold Coffee Company   DBA Gold Coffee Company, Gold Coffee Roasters, - 2009-04-15](https://www.keypedia.com/records/fda_inspections/costa-rican-gold-coffee-company-dba-gold-coffee-company-gold-coffee-roasters/91dcca99-4a87-4f6d-abd6-a04c704079fc) — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2009
- FDA Inspection 575801 - Costa Rican Gold Coffee Company   DBA Gold Coffee Company, Gold Coffee Roasters, - 2009-04-15 — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2009
- FDA Inspection 575801 - Costa Rican Gold Coffee Company   DBA Gold Coffee Company, Gold Coffee Roasters, - 2009-04-15 — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2009

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