# FDA Inspection 1026740 - VectraCor, Inc - September 27, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/vectracor-inc/4eab3a29-6fed-4b0d-bdfc-780b5f1a7d7a
Source feed: FDA_Inspections

> FDA Inspection 1026740 for VectraCor, Inc on September 27, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026740
- Company Name: VectraCor, Inc
- Inspection Date: 2017-09-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1026740 - 2017-09-27](https://www.globalkeysolutions.net/records/fda_inspections/vectracor-inc/6d38ca9d-e879-4252-afad-7fe26abd0668)
- [FDA Inspection 808583 - 2012-11-06](https://www.globalkeysolutions.net/records/fda_inspections/vectracor-inc/a65023cc-f46f-445a-89d1-fcdcc368e725)

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

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