# FDA Inspection 990051 - Leica Biosystems Newcastle Ltd - October 18, 2016

Source: https://www.keypedia.com/records/fda_inspections/leica-biosystems-newcastle-ltd/9339cb28-a165-4729-a452-d1c81bba9521
Source feed: FDA_Inspections

> FDA Inspection 990051 for Leica Biosystems Newcastle Ltd on October 18, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 990051
- Company Name: Leica Biosystems Newcastle Ltd
- Inspection Date: 2016-10-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 629608 - 2009-11-05](https://www.keypedia.com/records/fda_inspections/leica-biosystems-newcastle-ltd/a9d79415-233d-475a-83c5-d8d46fde4e60)

Company: https://www.keypedia.com/companies/leica-biosystems-newcastle-ltd/a5a63de3-a94b-4335-b6be-3466e621a543

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