# FDA Inspection 930102 - Herman H. Schroe, MD - April 24, 2015

Source: https://www.keypedia.com/records/fda_inspections/herman-h-schroe-md/26eeb3a1-a9d1-4689-aa87-210879f810be
Source feed: FDA_Inspections

> FDA Inspection 930102 for Herman H. Schroe, MD on April 24, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 930102
- Company Name: Herman H. Schroe, MD
- Inspection Date: 2015-04-24
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1107475 - 2019-10-25](https://www.keypedia.com/records/fda_inspections/herman-h-schroe-md/2e941c9c-3c14-47b9-8bca-a4189f88abd3)

Company: https://www.keypedia.com/companies/herman-h-schroe-md/8134697d-02fe-4283-8c7c-62530f42d262

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