# Larson Grain Company dba Farmer's Elevator - Inspection Records

Source: https://www.globalkeysolutions.net/companies/larson-grain-company-dba-farmers-elevator/dbbfe572-3e1d-4105-b49f-650bb3ffef21

> Inspection records and compliance data for Larson Grain Company dba Farmer's Elevator in Wishek, North Dakota. Access full analysis and detailed observations.

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## Details

- Name: Larson Grain Company dba Farmer's Elevator
- FEI Number: 1716410
- City: Wishek
- State: North Dakota
- Country Name: United States
- Address Line 1: 310 N Centennial St
- Zip Code: 58495

## Related Documents

- [FDA Inspection 1071664 - Larson Grain Company dba Farmer's Elevator - 2018-10-30](https://www.globalkeysolutions.net/records/fda_inspections/larson-grain-company-dba-farmers-elevator/98a5f370-f287-4ce6-bb11-9c4310060f90) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2018
- [FDA Inspection 1071664 - Larson Grain Company dba Farmer's Elevator - 2018-10-30](https://www.globalkeysolutions.net/records/fda_inspections/larson-grain-company-dba-farmers-elevator/b81ad197-142f-4c55-9d2f-a1db34a88091) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2018
- [FDA Inspection 876936 - Larson Grain Company dba Farmer's Elevator - 2014-04-09](https://www.globalkeysolutions.net/records/fda_inspections/larson-grain-company-dba-farmers-elevator/be2db360-2ef9-45a1-b5d2-d60aed0da5cf) — classification: No Action Indicated (NAI), source: FDA, date: April 9, 2014
- [FDA Inspection 720729 - Larson Grain Company dba Farmer's Elevator - 2011-04-05](https://www.globalkeysolutions.net/records/fda_inspections/larson-grain-company-dba-farmers-elevator/177c5956-6795-49b5-9908-8e9e27be10d4) — classification: No Action Indicated (NAI), source: FDA, date: April 5, 2011
- [FDA Inspection 593387 - Larson Grain Company dba Farmer's Elevator - 2009-06-16](https://www.globalkeysolutions.net/records/fda_inspections/larson-grain-company-dba-farmers-elevator/2492ef3a-ff81-4474-9ce1-3b8a144fefb8) — classification: No Action Indicated (NAI), source: FDA, date: June 16, 2009

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