# Meridian Medical Systems  LLC – FDA Inspection, Feb 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/meridian-medical-systems-llc/bc128304-fb8d-4d13-9ca6-63426f41b954
Source feed: FDA_Inspections

> FDA inspection 1002415 of Meridian Medical Systems  LLC, February 24, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002415
- Company Name: Meridian Medical Systems  LLC
- Inspection Date: 2017-02-24
- 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: 1

## Related Documents

- FDA Inspection 878130 - 2014-05-15
- [FDA Inspection 832897 - 2013-05-31](https://www.keypedia.com/records/fda_inspections/meridian-medical-systems-llc/ceee3a8d-d968-4318-ae1d-178984888f3b)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/benjamin-j-dastoli/688c2ad7-f7ac-47eb-8ca2-4efcd221f636)

Company: https://www.keypedia.com/companies/meridian-medical-systems-llc/d0e598f3-8e83-49b0-b743-8b0cceffcfa9

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