# Air Fayre CA, Inc., Gardena, CA – FDA Inspections

Source: https://www.keypedia.com/companies/air-fayre-ca-inc/02e5fde0-1f7f-4cdf-a5e2-bb88b7a7b138

> Inspection records and compliance data for Air Fayre CA, Inc. in Gardena, California. 13 FDA inspections on record, 1 Form 483, last inspected February 23, 2026.

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## Details

- Name: Air Fayre CA, Inc.
- FEI Number: 3013983652
- Address Line 1: 1720 W 135th St
- City: Gardena
- State: California
- Zip Code: 90249
- Country Name: United States
- Address: 1720 W 135th St, Gardena, California 90249, United States
- Country: United States

## Related Documents

- FDA Inspection 1304246 - Air Fayre CA, Inc. - 2026-02-23 — source: FDA, date: February 23, 2026
- [FDA Inspection 1304246 - Air Fayre CA, Inc. - 2026-02-23](https://www.keypedia.com/records/fda_inspections/air-fayre-ca-inc/e2bda04d-421d-4a63-96e0-9349aa31757e) — classification: No Action Indicated (NAI), source: FDA, date: February 23, 2026
- FDA Inspection 1304246 - Air Fayre CA, Inc. - 2026-02-23 — classification: No Action Indicated (NAI), source: FDA, date: February 23, 2026
- FDA Inspection 1269292 - Air Fayre CA, Inc. - 2025-04-15 — source: FDA, date: April 15, 2025
- [FDA Inspection 1269292 - Air Fayre CA, Inc. - 2025-04-15](https://www.keypedia.com/records/fda_inspections/air-fayre-ca-inc/7371db49-1ce3-4b44-a49f-970f8bbc41d7) — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2025
- FDA Inspection 1269292 - Air Fayre CA, Inc. - 2025-04-15 — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2025
- FDA Inspection 1155410 - Air Fayre CA, Inc. - 2021-10-27 — classification: No Action Indicated (NAI), source: FDA, date: October 27, 2021
- FDA Inspection 1155410 - Air Fayre CA, Inc. - 2021-10-27 — classification: No Action Indicated (NAI), source: FDA, date: October 27, 2021
- FDA Inspection 1102094 - Air Fayre CA, Inc. - 2019-08-19 — classification: No Action Indicated (NAI), source: FDA, date: August 19, 2019
- FDA Inspection 1102094 - Air Fayre CA, Inc. - 2019-08-19 — classification: No Action Indicated (NAI), source: FDA, date: August 19, 2019

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