# Leica Biosystems Newcastle Ltd. – FDA Inspection, Apr 27, 2017

Source: https://www.keypedia.com/records/fda_inspections/leica-biosystems-newcastle-ltd/a3a3c1be-ae78-46d9-bead-4495c5299463
Source feed: FDA_Inspections

> FDA inspection 1016878 of Leica Biosystems Newcastle Ltd., April 27, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016878
- Company Name: Leica Biosystems Newcastle Ltd.
- Inspection Date: 2017-04-27
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1093975 - 2019-01-25](https://www.keypedia.com/records/fda_inspections/leica-biosystems-newcastle-ltd/08367bdd-75b5-49d3-915d-1d00edf57683)
- FDA Inspection 883111 - 2014-06-05
- FDA Inspection 629656 - 2009-11-05

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)

Company: https://www.keypedia.com/companies/leica-biosystems-newcastle-ltd/b2f3453d-9261-46b6-9455-f1fe00be5a5a

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