# Coca-Cola Refreshments USA dba Odwalla,Inc., Dinuba, CA – FDA Inspections

Source: https://www.keypedia.com/companies/coca-cola-refreshments-usa-dba-odwallainc/5d0d061a-3657-4376-8115-abe97ac4304a

> Inspection records and compliance data for Coca-Cola Refreshments USA dba Odwalla,Inc. in Dinuba, California. 5 FDA inspections on record, last inspected June 04, 2015.

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## Details

- Name: Coca-Cola Refreshments USA dba Odwalla,Inc.
- FEI Number: 2939570
- Address Line 1: 1900 E Davis Dr
- City: Dinuba
- State: California
- Zip Code: 93618
- Country Name: United States
- Address: 1900 E Davis Dr, Dinuba, California 93618, United States
- Country: United States

## Related Documents

- [FDA Inspection 928307 - Coca-Cola Refreshments USA dba Odwalla,Inc. - 2015-06-04](https://www.keypedia.com/records/fda_inspections/coca-cola-refreshments-usa-dba-odwallainc/bb77893f-1477-4c73-aed7-9a810180300a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 4, 2015
- FDA Inspection 928307 - Coca-Cola Refreshments USA dba Odwalla,Inc. - 2015-06-04 — classification: No Action Indicated (NAI), source: FDA, date: June 4, 2015
- FDA Inspection 774156 - Coca-Cola Refreshments USA dba Odwalla,Inc. - 2012-04-04 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 4, 2012
- FDA Inspection 771816 - Coca-Cola Refreshments USA dba Odwalla,Inc. - 2012-03-12 — classification: No Action Indicated (NAI), source: FDA, date: March 12, 2012
- FDA Inspection 771816 - Coca-Cola Refreshments USA dba Odwalla,Inc. - 2012-03-12 — classification: No Action Indicated (NAI), source: FDA, date: March 12, 2012
- FDA Inspection 771816 - Coca-Cola Refreshments USA dba Odwalla,Inc. - 2012-03-12 — classification: No Action Indicated (NAI), source: FDA, date: March 12, 2012
- FDA Inspection 680405 - Coca-Cola Refreshments USA dba Odwalla,Inc. - 2010-09-14 — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2010
- FDA Inspection 610702 - Coca-Cola Refreshments USA dba Odwalla,Inc. - 2009-08-18 — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2009

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