# Xeridiem Medical Devices, Inc. – FDA Inspection, Feb 7, 2020

Source: https://www.keypedia.com/records/fda_inspections/xeridiem-medical-devices-inc/50f830c6-7e2e-4a9f-9cbd-ea72f86c5b72
Source feed: FDA_Inspections

> FDA inspection 1118179 of Xeridiem Medical Devices, Inc., February 07, 2020. Classification: Voluntary Action Indicated (VAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1118179
- Company Name: Xeridiem Medical Devices, Inc.
- Inspection Date: 2020-02-07
- 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: 0

## Related Documents

- [FDA Inspection 1158152 - 2019-07-12](https://www.keypedia.com/records/fda_inspections/xeridiem-medical-devices-inc/7c4915c2-8cbf-4e7f-95ed-0ab280959903)
- FDA Inspection 842401 - 2013-07-24

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

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