# Cardinal Health 414, LLC, Colton, CA – FDA Inspections

Source: https://www.keypedia.com/companies/cardinal-health-414-llc/2e2fae44-0591-4866-8698-a25c26d48f5b

> Inspection records and compliance data for Cardinal Health 414, LLC in Colton, California. 6 FDA inspections on record, 1 Form 483, last inspected June 26, 2025.

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## Details

- Name: Cardinal Health 414, LLC
- FEI Number: 3003411150
- Business Operations: POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION
- Address Line 1: 795 Via Lata
- City: Colton
- State: California
- Zip Code: 92324
- Country Name: United States
- Address: 795 Via Lata, Colton, California 92324, United States
- Country: United States

## Related Documents

- [FDA Inspection 1275955 - Cardinal Health 414, LLC - 2025-06-26](https://www.keypedia.com/records/fda_inspections/cardinal-health-414-llc/b4628112-d0da-460d-a65e-2941c4ac348b) — source: FDA, date: June 26, 2025
- FDA Inspection 1275955 - Cardinal Health 414, LLC - 2025-06-26 — classification: No Action Indicated (NAI), source: FDA, date: June 26, 2025
- [FDA Inspection 1049650 - Cardinal Health 414, LLC - 2018-04-20](https://www.keypedia.com/records/fda_inspections/cardinal-health-414-llc/8896f664-cdd7-4196-80ae-71770a24e93d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 20, 2018
- [FDA Inspection 877310 - Cardinal Health 414, LLC - 2014-05-01](https://www.keypedia.com/records/fda_inspections/cardinal-health-414-llc/465523f7-2030-4b61-b170-58ec0981ca1f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 1, 2014
- FDA Inspection 829631 - Cardinal Health 414, LLC - 2013-04-30 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 30, 2013
- [FDA Inspection 762739 - Cardinal Health 414, LLC - 2011-12-22](https://www.keypedia.com/records/fda_inspections/cardinal-health-414-llc/1a8042ff-4724-4b7a-8776-53417ae584eb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 22, 2011
- FDA Inspection 708489 - Cardinal Health 414, LLC - 2010-12-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 17, 2010

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