# FDA Inspection 973203 - Aerscher Diagnostics, LLC - June 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/aerscher-diagnostics-llc/8da6c171-2cbe-44fd-a1d7-bb9c07379286
Source feed: FDA_Inspections

> FDA Inspection 973203 for Aerscher Diagnostics, LLC on June 16, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 973203
- Company Name: Aerscher Diagnostics, LLC
- Inspection Date: 2016-06-16
- 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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Company: https://www.keypedia.com/companies/aerscher-diagnostics-llc/21faa930-755b-4beb-be2c-f031eb4f9348

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