# McKenna Labs Inc, Fullerton, CA – FDA Inspections

Source: https://www.keypedia.com/companies/mckenna-labs-inc/a0956f9d-e7ea-4bf6-ac78-77140586f684

> Inspection records and compliance data for McKenna Labs Inc in Fullerton, California. 5 FDA inspections on record, 2 Form 483s, last inspected February 13, 2025.

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## Details

- Name: McKenna Labs Inc
- FEI Number: 3003449422
- Address Line 1: 1601 E Orangethorpe Ave
- City: Fullerton
- State: California
- Zip Code: 92831
- Country Name: United States
- Address: 1601 E Orangethorpe Ave, Fullerton, California 92831, United States
- Country: United States

## Related Documents

- [483 - McKenna Labs Inc - 2025-02-13](https://www.keypedia.com/records/483/mckenna-labs-inc/ea984850-2d45-4f02-b6a3-a2eb070cd5d8) — source: FDA, date: February 13, 2025
- [FDA Inspection 1261255 - McKenna Labs Inc - 2025-02-13](https://www.keypedia.com/records/fda_inspections/mckenna-labs-inc/37032d5f-52ce-4287-847c-1a97a1b67ed2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 13, 2025
- [483 - McKenna Labs Inc - 2020-03-05](https://www.keypedia.com/records/483/mckenna-labs-inc/32371179-3cdc-4a14-b252-8918ed63e497) — source: FDA, date: March 5, 2020
- [FDA Inspection 1120409 - McKenna Labs Inc - 2020-03-05](https://www.keypedia.com/records/fda_inspections/mckenna-labs-inc/15a07c86-81d4-4444-8017-ae3f7c52ecf8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 5, 2020
- [FDA Inspection 1016911 - McKenna Labs Inc - 2017-07-05](https://www.keypedia.com/records/fda_inspections/mckenna-labs-inc/58803842-ed91-45aa-b0cd-4f1a4f91bc09) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 5, 2017
- FDA Inspection 702867 - McKenna Labs Inc - 2010-12-21 — classification: No Action Indicated (NAI), source: FDA, date: December 21, 2010
- FDA Inspection 541848 - McKenna Labs Inc - 2008-10-15 — classification: No Action Indicated (NAI), source: FDA, date: October 15, 2008
- FDA Inspection 541848 - McKenna Labs Inc - 2008-10-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 15, 2008

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