# AFP Advanced Food Products LLC, Visalia, CA – FDA Inspections

Source: https://www.keypedia.com/companies/afp-advanced-food-products-llc/9d283e0b-783b-4e88-b0d5-32dfdf3b9866

> Inspection records and compliance data for AFP Advanced Food Products LLC in Visalia, California. 4 FDA inspections on record, last inspected June 09, 2022.

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## Details

- Name: AFP Advanced Food Products LLC
- FEI Number: 3004341573
- Address Line 1: 2520 N Plaza Dr
- City: Visalia
- State: California
- Zip Code: 93291
- Country Name: United States
- Address: 2520 N Plaza Dr, Visalia, California 93291, United States
- Country: United States

## Related Documents

- FDA Inspection 1173670 - AFP Advanced Food Products LLC - 2022-06-09 — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2022
- FDA Inspection 1173670 - AFP Advanced Food Products LLC - 2022-06-09 — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2022
- FDA Inspection 1080696 - AFP Advanced Food Products LLC - 2019-01-31 — classification: No Action Indicated (NAI), source: FDA, date: January 31, 2019
- FDA Inspection 1080696 - AFP Advanced Food Products LLC - 2019-01-31 — classification: No Action Indicated (NAI), source: FDA, date: January 31, 2019
- FDA Inspection 768542 - AFP Advanced Food Products LLC - 2012-02-15 — classification: No Action Indicated (NAI), source: FDA, date: February 15, 2012
- FDA Inspection 768542 - AFP Advanced Food Products LLC - 2012-02-15 — classification: No Action Indicated (NAI), source: FDA, date: February 15, 2012
- FDA Inspection 768542 - AFP Advanced Food Products LLC - 2012-02-15 — classification: No Action Indicated (NAI), source: FDA, date: February 15, 2012
- FDA Inspection 768542 - AFP Advanced Food Products LLC - 2012-02-15 — classification: No Action Indicated (NAI), source: FDA, date: February 15, 2012
- FDA Inspection 608331 - AFP Advanced Food Products LLC - 2009-08-28 — classification: No Action Indicated (NAI), source: FDA, date: August 28, 2009
- FDA Inspection 608331 - AFP Advanced Food Products LLC - 2009-08-28 — classification: No Action Indicated (NAI), source: FDA, date: August 28, 2009

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