# FDA Inspection 979509 - Dierk Scheinert, MD - July 14, 2016

Source: https://www.keypedia.com/records/fda_inspections/dierk-scheinert-md/9ea61d44-2deb-4468-b1e9-d27d2793e3dc
Source feed: FDA_Inspections

> FDA Inspection 979509 for Dierk Scheinert, MD on July 14, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 979509
- Company Name: Dierk Scheinert, MD
- Inspection Date: 2016-07-14
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 876386 - 2014-03-27](https://www.keypedia.com/records/fda_inspections/dierk-scheinert-md/55d0b03d-dbfe-4e78-a7e5-e675e158bfa1)

Company: https://www.keypedia.com/companies/dierk-scheinert-md/4e50574d-dbf1-4e63-bf5c-c6c2a7c0d818

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