# Aspire Bakeries, LLC, Ontario, CA – FDA Inspections

Source: https://www.keypedia.com/companies/aspire-bakeries-llc/14725577-e789-4ff3-951d-473b401ad555

> Inspection records and compliance data for Aspire Bakeries, LLC in Ontario, California. 5 FDA inspections on record, last inspected July 23, 2025.

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## Details

- Name: Aspire Bakeries, LLC
- FEI Number: 3006611192
- Address Line 1: 1220 S Baker Ave
- City: Ontario
- State: California
- Zip Code: 91761
- Country Name: United States
- Address: 1220 S Baker Ave, Ontario, California 91761, United States
- Country: United States

## Related Documents

- FDA Inspection 1277022 - Aspire Bakeries, LLC - 2025-07-23 — source: FDA, date: July 23, 2025
- FDA Inspection 1277022 - Aspire Bakeries, LLC - 2025-07-23 — source: FDA, date: July 23, 2025
- FDA Inspection 1277022 - Aspire Bakeries, LLC - 2025-07-23 — classification: No Action Indicated (NAI), source: FDA, date: July 23, 2025
- [FDA Inspection 1277022 - Aspire Bakeries, LLC - 2025-07-23](https://www.keypedia.com/records/fda_inspections/aspire-bakeries-llc/ab70841e-2d36-46c3-9b0c-e402fc7538b6) — classification: No Action Indicated (NAI), source: FDA, date: July 23, 2025
- FDA Inspection 1277022 - Aspire Bakeries, LLC - 2025-07-23 — classification: No Action Indicated (NAI), source: FDA, date: July 23, 2025
- [FDA Inspection 1191795 - Aspire Bakeries, LLC - 2022-12-01](https://www.keypedia.com/records/fda_inspections/aspire-bakeries-llc/3eaf7f7b-6d43-483d-ab53-774b8700997e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 1, 2022
- FDA Inspection 1105461 - Aspire Bakeries, LLC - 2019-09-26 — source: FDA, date: September 26, 2019
- FDA Inspection 1028809 - Aspire Bakeries, LLC - 2017-09-27 — classification: No Action Indicated (NAI), source: FDA, date: September 27, 2017
- FDA Inspection 1028809 - Aspire Bakeries, LLC - 2017-09-27 — classification: No Action Indicated (NAI), source: FDA, date: September 27, 2017
- FDA Inspection 861217 - Aspire Bakeries, LLC - 2013-11-01 — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2013

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