# FDA Inspection 842401 - Xeridiem Medical Devices, Inc. - July 24, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/xeridiem-medical-devices-inc/c5445018-7730-43fb-a6df-8ab02d6cf1ff
Source feed: FDA_Inspections

> FDA Inspection 842401 for Xeridiem Medical Devices, Inc. on July 24, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 842401
- Company Name: Xeridiem Medical Devices, Inc.
- Inspection Date: 2013-07-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1118179 - 2020-02-07](https://www.globalkeysolutions.net/records/fda_inspections/xeridiem-medical-devices-inc/50f830c6-7e2e-4a9f-9cbd-ea72f86c5b72)

Company: https://www.globalkeysolutions.net/companies/xeridiem-medical-devices-inc/9a455ccf-9d0a-42ee-9a96-4ca57f90bf4d

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