# VectraCor, Inc – FDA Inspection, Sep 27, 2017

Source: https://www.keypedia.com/records/fda_inspections/vectracor-inc/6d38ca9d-e879-4252-afad-7fe26abd0668
Source feed: FDA_Inspections

> FDA inspection 1026740 of VectraCor, Inc, September 27, 2017. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026740
- Company Name: VectraCor, Inc
- Inspection Date: 2017-09-27
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 808583 - 2012-11-06](https://www.keypedia.com/records/fda_inspections/vectracor-inc/a65023cc-f46f-445a-89d1-fcdcc368e725)

## Related Officers

- Melissa A. Zuppe

Company: https://www.keypedia.com/companies/vectracor-inc/36c25c0d-2839-405e-a06a-810e15de2af5

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