# FDA Inspection 1193146 - Louisville APL Diagnostics, Inc. - December 19, 2022

Source: https://www.globalkeysolutions.net/records/fda_inspections/louisville-apl-diagnostics-inc/f91083fb-a846-40ab-84fd-3059a8a215d1/
Source feed: FDA_Inspections

> FDA Inspection 1193146 for Louisville APL Diagnostics, Inc. on December 19, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1193146
- Company Name: Louisville APL Diagnostics, Inc.
- Inspection Date: 2022-12-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1193146 - 2022-12-19](https://www.globalkeysolutions.net/api/records/fda_inspections/louisville-apl-diagnostics-inc/9f5d0e72-f933-4a04-8adb-65de04bf3e4b/)
- [FDA Inspection 1012564 - 2017-06-02](https://www.globalkeysolutions.net/api/records/fda_inspections/louisville-apl-diagnostics-inc/0e68a4ff-8148-4f3a-b062-841c23cf391e/)
- [FDA Inspection 945280 - 2015-08-03](https://www.globalkeysolutions.net/api/records/fda_inspections/louisville-apl-diagnostics-inc/820e8e5c-f545-4475-9391-56431b575042/)
- [FDA Inspection 945280 - 2015-08-03](https://www.globalkeysolutions.net/api/records/fda_inspections/louisville-apl-diagnostics-inc/baa61ee3-b4d2-4b37-966b-6ada4814c131/)

Company: https://www.globalkeysolutions.net/companies/louisville-apl-diagnostics-inc/40244cc1-a098-48d3-9ca2-7eb649e56a65

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