# Vitalcor, Inc. – FDA Inspection, Jan 11, 2017

Source: https://www.keypedia.com/records/fda_inspections/vitalcor-inc/8fe98f6a-4db9-4d47-a625-a8fdc10b2279
Source feed: FDA_Inspections

> FDA inspection 1005602 of Vitalcor, Inc., January 11, 2017. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1005602
- Company Name: Vitalcor, Inc.
- Inspection Date: 2017-01-11
- 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: 8

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brittani-n-franklin/1d5e9344-1145-42ff-a175-5541b565b15e)

Company: https://www.keypedia.com/companies/vitalcor-inc/2276a926-ba6a-4477-967a-be320917b5ad

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