# Cardinal Health 414 LLC, Beltsville, MD – FDA Inspections

Source: https://www.keypedia.com/companies/cardinal-health-414-llc/c4962210-1c42-46f3-82af-148e17b24e79

> Inspection records and compliance data for Cardinal Health 414 LLC in Beltsville, Maryland. 6 FDA inspections on record, last inspected January 09, 2024.

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## Details

- Name: Cardinal Health 414 LLC
- FEI Number: 3004612405
- Business Operations: POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION
- Address Line 1: 7051 Muirkirk Meadows Dr Ste L
- City: Beltsville
- State: Maryland
- Zip Code: 20705
- Country Name: United States
- Address: 7051 Muirkirk Meadows Dr Ste L, Beltsville, Maryland 20705, United States
- Country: United States

## Related Documents

- [483 - Cardinal Health 414 LLC - 2024-01-09](https://www.keypedia.com/records/483/cardinal-health-414-llc/b0854d42-6b3c-4069-81ae-0e00dd9f4d85) — source: FDA, date: January 9, 2024
- [FDA Inspection 1226823 - Cardinal Health 414 LLC - 2024-01-09](https://www.keypedia.com/records/fda_inspections/cardinal-health-414-llc/0cceea96-8fad-4efa-9bd6-735ddcc92243) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 9, 2024
- FDA Inspection 999780 - Cardinal Health 414 LLC - 2016-09-30 — classification: No Action Indicated (NAI), source: FDA, date: September 30, 2016
- [FDA Inspection 862870 - Cardinal Health 414 LLC - 2014-01-17](https://www.keypedia.com/records/fda_inspections/cardinal-health-414-llc/9fed2fe8-4c60-4f37-b123-e977d9b76293) — classification: No Action Indicated (NAI), source: FDA, date: January 17, 2014
- FDA Inspection 773084 - Cardinal Health 414 LLC - 2012-03-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 20, 2012
- [FDA Inspection 628986 - Cardinal Health 414 LLC - 2009-11-13](https://www.keypedia.com/records/fda_inspections/cardinal-health-414-llc/225589c6-582e-467b-bc90-871abc529696) — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2009
- FDA Inspection 556151 - Cardinal Health 414 LLC - 2009-01-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 15, 2009

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