# FDA Inspection 819998 - Harold L. Dauerman, M.D. - February 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/harold-l-dauerman-md/cf5f17ef-a361-4f04-ae5d-7e32fc0c0390
Source feed: FDA_Inspections

> FDA Inspection 819998 for Harold L. Dauerman, M.D. on February 26, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 819998
- Company Name: Harold L. Dauerman, M.D.
- Inspection Date: 2013-02-26
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/harold-l-dauerman-md/22213d66-f195-4d33-a38a-bb4c23cf104d

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