# Medi-Source Inc – FDA Inspection, Jul 11, 2017

Source: https://www.keypedia.com/records/fda_inspections/medi-source-inc/d042c933-f1f8-4f8d-8bd8-b181fcde5006
Source feed: FDA_Inspections

> FDA inspection 1017923 of Medi-Source Inc, July 11, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations 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: 1017923
- Company Name: Medi-Source Inc
- Inspection Date: 2017-07-11
- 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: 2

## Related Documents

- FDA Inspection 922180 - 2015-04-13
- FDA Inspection 673049 - 2010-07-23

## Related Officers

- [Company Rep](https://www.keypedia.com/people/javonica-f-penn/56294265-08fc-4d1d-8a34-626fc4dad457)

Company: https://www.keypedia.com/companies/medi-source-inc/df256c6c-f168-467d-8ad2-eaea5563ee2a

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