# FDA Inspection 844881 - Leica Biosystems Imaging, Inc. - August 07, 2013

Source: https://www.keypedia.com/records/fda_inspections/leica-biosystems-imaging-inc/58e440e4-c5ee-4689-a117-5dfae78d2706
Source feed: FDA_Inspections

> FDA Inspection 844881 for Leica Biosystems Imaging, Inc. on August 07, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 844881
- Company Name: Leica Biosystems Imaging, Inc.
- Inspection Date: 2013-08-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 928828 - 2015-02-06](https://www.keypedia.com/records/fda_inspections/leica-biosystems-imaging-inc/322ec491-a8db-4d2e-88c0-32b64223b2c4)
- [FDA Inspection 844881 - 2013-08-07](https://www.keypedia.com/records/fda_inspections/leica-biosystems-imaging-inc/e5072331-ead9-451f-879d-168c3fa4c989)

Company: https://www.keypedia.com/companies/leica-biosystems-imaging-inc/0cff0cda-e7db-42be-8e2a-34036f6a9504

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