# Clearwater Fine Foods USA Inc, Louisville, KY – FDA Inspections

Source: https://www.keypedia.com/companies/clearwater-fine-foods-usa-inc/25a207a1-54b4-44ad-85fa-351e53546eef

> Inspection records and compliance data for Clearwater Fine Foods USA Inc in Louisville, Kentucky. 5 FDA inspections on record, last inspected March 23, 2017.

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## Details

- Name: Clearwater Fine Foods USA Inc
- FEI Number: 3002849258
- Address Line 1: 3904 Produce Rd Ste 103
- City: Louisville
- State: Kentucky
- Zip Code: 40218
- Country Name: United States
- Address: 3904 Produce Rd Ste 103, Louisville, Kentucky 40218, United States
- Country: United States

## Related Documents

- FDA Inspection 1005994 - Clearwater Fine Foods USA Inc - 2017-03-23 — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2017
- FDA Inspection 1005994 - Clearwater Fine Foods USA Inc - 2017-03-23 — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2017
- FDA Inspection 871534 - Clearwater Fine Foods USA Inc - 2014-03-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 26, 2014
- FDA Inspection 854463 - Clearwater Fine Foods USA Inc - 2013-11-07 — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2013
- FDA Inspection 854463 - Clearwater Fine Foods USA Inc - 2013-11-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 7, 2013
- FDA Inspection 854463 - Clearwater Fine Foods USA Inc - 2013-11-07 — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2013
- [FDA Inspection 732058 - Clearwater Fine Foods USA Inc - 2011-06-29](https://www.keypedia.com/records/fda_inspections/clearwater-fine-foods-usa-inc/bae48583-2858-4af4-95c7-aa910a5592f2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2011
- [FDA Inspection 667360 - Clearwater Fine Foods USA Inc - 2010-06-16](https://www.keypedia.com/records/fda_inspections/clearwater-fine-foods-usa-inc/ebb0a996-b73c-484c-9802-c2fdf6f80ddf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 16, 2010

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