# BioFire Diagnostics, LLC – FDA Inspection, Apr 5, 2024

Source: https://www.keypedia.com/records/fda_inspections/biofire-diagnostics-llc/931b5488-77d8-46c5-a296-354d10ab443c
Source feed: FDA_Inspections

> FDA inspection 1235522 of BioFire Diagnostics, LLC, April 05, 2024. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1235522
- Company Name: BioFire Diagnostics, LLC
- Inspection Date: 2024-04-05
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1148989 - 2021-08-05
- FDA Inspection 1082140 - 2018-05-15
- [FDA Inspection 1046822 - 2017-10-23](https://www.keypedia.com/records/fda_inspections/biofire-diagnostics-llc/150dcba7-6114-45f3-a9ed-a1050e7e6f9b)
- FDA Inspection 1045120 - 2017-10-23
- FDA Inspection 964419 - 2016-03-18

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

Company: https://www.keypedia.com/companies/biofire-diagnostics-llc/42f061ce-087c-4ae8-ab03-752cae683764

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7