# Frito-Lay, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/frito-lay-inc/7ae07eb9-9a64-48a8-923f-748decb83a13

> Inspection records and compliance data for Frito-Lay, Inc. in Irving, Texas. Access full analysis and detailed observations.

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## Details

- Name: Frito-Lay, Inc.
- FEI Number: 1611049
- City: Irving
- State: Texas
- Country Name: United States
- Address Line 1: 701 N Wildwood Dr
- Zip Code: 75061

## Related Documents

- [FDA Inspection 1151903 - Frito-Lay, Inc. - 2021-09-02](https://www.keypedia.com/records/fda_inspections/frito-lay-inc/f1451695-a09f-4d4b-a4cf-9753b1d1dd4f) — classification: No Action Indicated (NAI), source: FDA, date: September 2, 2021
- [FDA Inspection 1096506 - Frito-Lay, Inc. - 2019-07-12](https://www.keypedia.com/records/fda_inspections/frito-lay-inc/d289a374-5d8d-430d-8116-409a6d6effe8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 12, 2019
- [FDA Inspection 1091205 - Frito-Lay, Inc. - 2019-05-14](https://www.keypedia.com/records/fda_inspections/frito-lay-inc/051d29ba-768b-4737-93b0-f8c8c2fbae71) — classification: No Action Indicated (NAI), source: FDA, date: May 14, 2019
- [FDA Inspection 641503 - Frito-Lay, Inc. - 2010-01-26](https://www.keypedia.com/records/fda_inspections/frito-lay-inc/57ca386e-1404-4660-a445-e4be9f20ba21) — classification: No Action Indicated (NAI), source: FDA, date: January 26, 2010
- [FDA Inspection 641503 - Frito-Lay, Inc. - 2010-01-26](https://www.keypedia.com/records/fda_inspections/frito-lay-inc/68351eb8-53c9-4a51-8c64-082da1d5e8a7) — classification: No Action Indicated (NAI), source: FDA, date: January 26, 2010
- [FDA Inspection 641503 - Frito-Lay, Inc. - 2010-01-26](https://www.keypedia.com/records/fda_inspections/frito-lay-inc/6dc0c158-e811-4807-8fb6-314d243cfca0) — classification: No Action Indicated (NAI), source: FDA, date: January 26, 2010
- [FDA Inspection 641503 - Frito-Lay, Inc. - 2010-01-26](https://www.keypedia.com/records/fda_inspections/frito-lay-inc/730e3889-6703-495d-aa3e-6ac4f90759a3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 26, 2010

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