# FDA Inspection 823260 - Stefan W. Kreuzer, MD - March 08, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/stefan-w-kreuzer-md/11d167de-9dca-409d-8104-69aaf3435724
Source feed: FDA_Inspections

> FDA Inspection 823260 for Stefan W. Kreuzer, MD on March 08, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 823260
- Company Name: Stefan W. Kreuzer, MD
- Inspection Date: 2013-03-08
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1099416 - 2019-08-13](https://www.globalkeysolutions.net/records/fda_inspections/stefan-w-kreuzer-md/3caff309-25b4-44a2-aff7-e26aab5a1fef)

Company: https://www.globalkeysolutions.net/companies/stefan-w-kreuzer-md/9a806cb8-a3f1-4c80-bacf-d16a4690635b

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