# FDA Inspection 554382 - Janssen Diagnostics, LLC - December 17, 2008

Source: https://www.keypedia.com/records/fda_inspections/janssen-diagnostics-llc/6ff62c67-7695-4a05-bfa2-7cf86e9e913e
Source feed: FDA_Inspections

> FDA Inspection 554382 for Janssen Diagnostics, LLC on December 17, 2008. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 554382
- Company Name: Janssen Diagnostics, LLC
- Inspection Date: 2008-12-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 554382 - 2008-12-17](https://www.keypedia.com/records/fda_inspections/janssen-diagnostics-llc/7ff90668-e13f-450e-abd9-0a337db42598)

Company: https://www.keypedia.com/companies/janssen-diagnostics-llc/e52062d9-0d31-473f-be1b-c013480238a7

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