# Hildebrand Farms Inc, Junction City, KS – FDA Inspections

Source: https://www.keypedia.com/companies/hildebrand-farms-inc/ab6d520f-ea40-4fe2-81bc-129838012826

> Inspection records and compliance data for Hildebrand Farms Inc in Junction City, Kansas. 6 FDA inspections on record, last inspected January 28, 2025.

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## Details

- Name: Hildebrand Farms Inc
- FEI Number: 3007033507
- Address Line 1: 5210 Rucker Rd
- City: Junction City
- State: Kansas
- Zip Code: 66441
- Country Name: United States
- Address: 5210 Rucker Rd, Junction City, Kansas 66441, United States
- Country: United States

## Related Documents

- FDA Inspection 1262566 - Hildebrand Farms Inc - 2025-01-28 — source: FDA, date: January 28, 2025
- FDA Inspection 1262566 - Hildebrand Farms Inc - 2025-01-28 — classification: No Action Indicated (NAI), source: FDA, date: January 28, 2025
- [FDA Inspection 1262566 - Hildebrand Farms Inc - 2025-01-28](https://www.keypedia.com/records/fda_inspections/hildebrand-farms-inc/a043da39-10e2-4e32-808f-bf5bfde3b679) — classification: No Action Indicated (NAI), source: FDA, date: January 28, 2025
- FDA Inspection 1174772 - Hildebrand Farms Inc - 2022-06-23 — classification: No Action Indicated (NAI), source: FDA, date: June 23, 2022
- FDA Inspection 951822 - Hildebrand Farms Inc - 2015-10-20 — classification: No Action Indicated (NAI), source: FDA, date: October 20, 2015
- FDA Inspection 951822 - Hildebrand Farms Inc - 2015-10-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 20, 2015
- FDA Inspection 712673 - Hildebrand Farms Inc - 2011-01-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 26, 2011
- [FDA Inspection 668051 - Hildebrand Farms Inc - 2010-05-26](https://www.keypedia.com/records/fda_inspections/hildebrand-farms-inc/1a5c69d8-6fab-4d13-b6f1-273514bd651b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 26, 2010
- FDA Inspection 668073 - Hildebrand Farms Inc - 2010-02-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 11, 2010

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