# F. Alioto Co., Inc., San Francisco, CA – FDA Inspections

Source: https://www.keypedia.com/companies/f-alioto-co-inc/14ffefce-547b-440b-aab7-2d72756d9944

> Inspection records and compliance data for F. Alioto Co., Inc. in San Francisco, California. 6 FDA inspections on record, 1 Form 483, last inspected July 01, 2025.

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## Details

- Name: F. Alioto Co., Inc.
- FEI Number: 2916513
- Address Line 1: 440 Jefferson St
- City: San Francisco
- State: California
- Zip Code: 94109
- Country Name: United States
- Address: 440 Jefferson St, San Francisco, California 94109, United States
- Country: United States

## Related Documents

- FDA Inspection 1274441 - F. Alioto Co., Inc. - 2025-07-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 1, 2025
- [FDA Inspection 1274441 - F. Alioto Co., Inc. - 2025-07-01](https://www.keypedia.com/records/fda_inspections/f-alioto-co-inc/26146445-482c-403e-b2ee-201853630cd0) — classification: No Action Indicated (NAI), source: FDA, date: July 1, 2025
- FDA Inspection 1274441 - F. Alioto Co., Inc. - 2025-07-01 — classification: No Action Indicated (NAI), source: FDA, date: July 1, 2025
- FDA Inspection 1177553 - F. Alioto Co., Inc. - 2022-07-27 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 27, 2022
- FDA Inspection 1177553 - F. Alioto Co., Inc. - 2022-07-27 — classification: No Action Indicated (NAI), source: FDA, date: July 27, 2022
- FDA Inspection 1039211 - F. Alioto Co., Inc. - 2017-12-19 — classification: No Action Indicated (NAI), source: FDA, date: December 19, 2017
- [FDA Inspection 910442 - F. Alioto Co., Inc. - 2015-01-14](https://www.keypedia.com/records/fda_inspections/f-alioto-co-inc/ec21f3cf-d3c3-4349-a5d5-c96448761a8e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 14, 2015
- FDA Inspection 787824 - F. Alioto Co., Inc. - 2012-06-21 — classification: No Action Indicated (NAI), source: FDA, date: June 21, 2012
- FDA Inspection 629553 - F. Alioto Co., Inc. - 2009-11-18 — classification: No Action Indicated (NAI), source: FDA, date: November 18, 2009

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