# FDA Inspection 1050360 - Kirk Voelker, MD - April 12, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/kirk-voelker-md/06367b07-6f5e-44b2-8ae6-9dea56df1998
Source feed: FDA_Inspections

> FDA Inspection 1050360 for Kirk Voelker, MD on April 12, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1050360
- Company Name: Kirk Voelker, MD
- Inspection Date: 2018-04-12
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 766712 - 2012-02-02](https://www.globalkeysolutions.net/records/fda_inspections/kirk-voelker-md/d68e1e83-9aeb-4e82-8a34-83c364d73470)

Company: https://www.globalkeysolutions.net/companies/kirk-voelker-md/57908556-314f-4801-885b-8ab1b74ae414

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