# Honeyville Inc - Inspection Records

Source: https://www.globalkeysolutions.net/companies/honeyville-inc/132e06a5-41aa-4604-9b97-bac35631ce3a

> Inspection records and compliance data for Honeyville Inc in Rancho Cucamonga, California. Access full analysis and detailed observations.

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## Details

- Name: Honeyville Inc
- FEI Number: 2024136
- City: Rancho Cucamonga
- State: California
- Country Name: United States
- Address Line 1: 11600 Dayton Dr
- Zip Code: 91730

## Related Documents

- [FDA Inspection 1153171 - Honeyville Inc - 2021-09-01](https://www.globalkeysolutions.net/records/fda_inspections/honeyville-inc/34508ec0-b9a7-4b60-8793-b75113b10676) — classification: No Action Indicated (NAI), source: FDA, date: September 1, 2021
- [FDA Inspection 1153171 - Honeyville Inc - 2021-09-01](https://www.globalkeysolutions.net/records/fda_inspections/honeyville-inc/728c3fea-57d5-4d47-90fe-3cc7c1ad7d78) — classification: No Action Indicated (NAI), source: FDA, date: September 1, 2021
- [FDA Inspection 721837 - Honeyville Inc - 2011-04-26](https://www.globalkeysolutions.net/records/fda_inspections/honeyville-inc/da5a2752-9fe6-42fa-aded-2c41a6a3b50b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 26, 2011
- [FDA Inspection 721837 - Honeyville Inc - 2011-04-26](https://www.globalkeysolutions.net/records/fda_inspections/honeyville-inc/8031c97c-0d21-43f7-a9b4-3ca2424e57bc) — classification: No Action Indicated (NAI), source: FDA, date: April 26, 2011
- [FDA Inspection 735993 - Honeyville Inc - 2010-10-25](https://www.globalkeysolutions.net/records/fda_inspections/honeyville-inc/0e4944d2-099e-4eac-b135-9fb78480a7c9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 25, 2010
- [FDA Inspection 652443 - Honeyville Inc - 2010-02-17](https://www.globalkeysolutions.net/records/fda_inspections/honeyville-inc/2d8161ae-dfdf-4919-a830-323f883797eb) — classification: No Action Indicated (NAI), source: FDA, date: February 17, 2010
- [FDA Inspection 652443 - Honeyville Inc - 2010-02-17](https://www.globalkeysolutions.net/records/fda_inspections/honeyville-inc/c338fd6a-599d-4b7f-953e-33c4fc1c7ccb) — classification: No Action Indicated (NAI), source: FDA, date: February 17, 2010

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