# The Coffee Connexion Co., Inc, Lebanon, TN – FDA Inspections

Source: https://www.keypedia.com/companies/the-coffee-connexion-co-inc/36794ce0-cd77-4acd-a830-944ee0b85efc

> Inspection records and compliance data for The Coffee Connexion Co., Inc in Lebanon, Tennessee. 7 FDA inspections on record, last inspected January 05, 2024.

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## Details

- Name: The Coffee Connexion Co., Inc
- FEI Number: 3011182588
- Address Line 1: 216 E Main St
- City: Lebanon
- State: Tennessee
- Zip Code: 37087
- Country Name: United States
- Address: 216 E Main St, Lebanon, Tennessee 37087, United States
- Country: United States

## Related Documents

- FDA Inspection 1231127 - The Coffee Connexion Co., Inc - 2024-01-05 — source: FDA, date: January 5, 2024
- FDA Inspection 1078069 - The Coffee Connexion Co., Inc - 2019-01-17 — source: FDA, date: January 17, 2019
- FDA Inspection 1037393 - The Coffee Connexion Co., Inc - 2017-12-14 — source: FDA, date: December 14, 2017
- FDA Inspection 975155 - The Coffee Connexion Co., Inc - 2016-05-19 — classification: No Action Indicated (NAI), source: FDA, date: May 19, 2016
- FDA Inspection 975155 - The Coffee Connexion Co., Inc - 2016-05-19 — classification: No Action Indicated (NAI), source: FDA, date: May 19, 2016
- FDA Inspection 975155 - The Coffee Connexion Co., Inc - 2016-05-19 — classification: No Action Indicated (NAI), source: FDA, date: May 19, 2016
- [FDA Inspection 804716 - The Coffee Connexion Co., Inc - 2012-10-25](https://www.keypedia.com/records/fda_inspections/the-coffee-connexion-co-inc/ee8a0391-91bf-4828-8004-e58ac92e4da2) — classification: No Action Indicated (NAI), source: FDA, date: October 25, 2012
- FDA Inspection 804716 - The Coffee Connexion Co., Inc - 2012-10-25 — classification: No Action Indicated (NAI), source: FDA, date: October 25, 2012
- FDA Inspection 804716 - The Coffee Connexion Co., Inc - 2012-10-25 — classification: No Action Indicated (NAI), source: FDA, date: October 25, 2012
- FDA Inspection 667038 - The Coffee Connexion Co., Inc - 2010-06-03 — classification: No Action Indicated (NAI), source: FDA, date: June 3, 2010

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