# Wawona Frozen Foods, Fresno, CA – FDA Inspections

Source: https://www.keypedia.com/companies/wawona-frozen-foods/412c4477-3cff-4641-9e97-96479ded8a57

> Inspection records and compliance data for Wawona Frozen Foods in Fresno, California. 3 FDA inspections on record, last inspected September 17, 2019.

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## Details

- Name: Wawona Frozen Foods
- FEI Number: 3004383099
- Address Line 1: 2202 S Cedar Ave
- City: Fresno
- State: California
- Zip Code: 93725
- Country Name: United States
- Address: 2202 S Cedar Ave, Fresno, California 93725, United States
- Country: United States

## Related Documents

- FDA Inspection 1110107 - Wawona Frozen Foods - 2019-09-17 — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2019
- FDA Inspection 1110107 - Wawona Frozen Foods - 2019-09-17 — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2019
- FDA Inspection 896814 - Wawona Frozen Foods - 2014-09-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 24, 2014
- FDA Inspection 896814 - Wawona Frozen Foods - 2014-09-24 — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2014
- FDA Inspection 896814 - Wawona Frozen Foods - 2014-09-24 — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2014
- FDA Inspection 896814 - Wawona Frozen Foods - 2014-09-24 — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2014
- [FDA Inspection 896814 - Wawona Frozen Foods - 2014-09-24](https://www.keypedia.com/records/fda_inspections/wawona-frozen-foods/dd26f326-3a33-4de9-b35f-188684a7b89f) — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2014
- FDA Inspection 749363 - Wawona Frozen Foods - 2011-10-13 — classification: No Action Indicated (NAI), source: FDA, date: October 13, 2011
- FDA Inspection 749363 - Wawona Frozen Foods - 2011-10-13 — classification: No Action Indicated (NAI), source: FDA, date: October 13, 2011
- FDA Inspection 749363 - Wawona Frozen Foods - 2011-10-13 — classification: No Action Indicated (NAI), source: FDA, date: October 13, 2011

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