# Frontier Ag, Inc., Grinnell, KS – FDA Inspections

Source: https://www.keypedia.com/companies/frontier-ag-inc/a21a795c-cea8-4cb9-aa5b-668402f8b389

> Inspection records and compliance data for Frontier Ag, Inc. in Grinnell, Kansas. 9 FDA inspections on record (1 OAI), last inspected February 25, 2025.

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## Details

- Name: Frontier Ag, Inc.
- FEI Number: 1912225
- Address Line 1: 200 Railroad Ave
- City: Grinnell
- State: Kansas
- Zip Code: 67738
- Country Name: United States
- Address: 200 Railroad Ave, Grinnell, Kansas 67738, United States
- Country: United States

## Related Documents

- FDA Inspection 1262924 - Frontier Ag, Inc. - 2025-02-25 — source: FDA, date: February 25, 2025
- FDA Inspection 1262924 - Frontier Ag, Inc. - 2025-02-25 — classification: No Action Indicated (NAI), source: FDA, date: February 25, 2025
- FDA Inspection 1233008 - Frontier Ag, Inc. - 2024-02-29 — classification: No Action Indicated (NAI), source: FDA, date: February 29, 2024
- FDA Inspection 1197960 - Frontier Ag, Inc. - 2023-02-07 — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2023
- [FDA Inspection 1169568 - Frontier Ag, Inc. - 2022-05-11](https://www.keypedia.com/records/fda_inspections/frontier-ag-inc/697bccbe-ceec-4948-bb24-962c275c2988) — classification: Official Action Indicated (OAI), source: FDA, date: May 11, 2022
- FDA Inspection 1145949 - Frontier Ag, Inc. - 2021-06-21 — classification: No Action Indicated (NAI), source: FDA, date: June 21, 2021
- [FDA Inspection 1086874 - Frontier Ag, Inc. - 2019-03-07](https://www.keypedia.com/records/fda_inspections/frontier-ag-inc/6c54c64c-5790-4798-88c4-40ad01756f4f) — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2019
- FDA Inspection 899947 - Frontier Ag, Inc. - 2014-09-24 — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2014
- FDA Inspection 735452 - Frontier Ag, Inc. - 2011-07-20 — classification: No Action Indicated (NAI), source: FDA, date: July 20, 2011
- FDA Inspection 604831 - Frontier Ag, Inc. - 2009-08-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 6, 2009

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