# Del Monte Fresh Produce N.A., Inc. - Inspection Records

Source: https://www.keypedia.com/companies/del-monte-fresh-produce-na-inc/edce7bb7-caad-4a47-bd7a-00d55358e680

> Inspection records and compliance data for Del Monte Fresh Produce N.A., Inc. in Kankakee, Illinois. 11 FDA inspections on record, last inspected April 02, 2026.

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## Details

- Name: Del Monte Fresh Produce N.A., Inc.
- FEI Number: 1000114937
- Address Line 1: 14 Stuart Dr
- City: Kankakee
- State: Illinois
- Zip Code: 60901
- Country Name: United States
- Address: 14 Stuart Dr, Kankakee, Illinois 60901, United States
- Country: United States

## Related Documents

- FDA Inspection 1312794 - Del Monte Fresh Produce N.A., Inc. - 2026-04-02 — classification: No Action Indicated (NAI), source: FDA, date: April 2, 2026
- FDA Inspection 1260517 - Del Monte Fresh Produce N.A., Inc. - 2025-01-09 — source: FDA, date: January 9, 2025
- FDA Inspection 1205728 - Del Monte Fresh Produce N.A., Inc. - 2023-04-26 — classification: No Action Indicated (NAI), source: FDA, date: April 26, 2023
- FDA Inspection 1205728 - Del Monte Fresh Produce N.A., Inc. - 2023-04-26 — classification: No Action Indicated (NAI), source: FDA, date: April 26, 2023
- FDA Inspection 1098294 - Del Monte Fresh Produce N.A., Inc. - 2019-07-18 — classification: No Action Indicated (NAI), source: FDA, date: July 18, 2019
- FDA Inspection 1098294 - Del Monte Fresh Produce N.A., Inc. - 2019-07-18 — classification: No Action Indicated (NAI), source: FDA, date: July 18, 2019
- FDA Inspection 1092016 - Del Monte Fresh Produce N.A., Inc. - 2019-06-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 6, 2019
- FDA Inspection 1092016 - Del Monte Fresh Produce N.A., Inc. - 2019-06-06 — classification: No Action Indicated (NAI), source: FDA, date: June 6, 2019
- FDA Inspection 1065413 - Del Monte Fresh Produce N.A., Inc. - 2018-08-14 — classification: No Action Indicated (NAI), source: FDA, date: August 14, 2018
- FDA Inspection 1008348 - Del Monte Fresh Produce N.A., Inc. - 2017-03-16 — classification: No Action Indicated (NAI), source: FDA, date: March 16, 2017

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